Trial Outcomes & Findings for Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for the Treatment of SFA and Proximal Popliteal Arterial Disease (NCT NCT01175850)

NCT ID: NCT01175850

Last Updated: 2017-05-16

Results Overview

Primary patency is defined as freedom from clinically-driven target lesion revascularization (TLR) or restenosis as determined by duplex ultrasound (DUS) Peak Systolic Velocity Ratio (PSVR) ≤ 2.4.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

331 participants

Primary outcome timeframe

12 Month

Results posted on

2017-05-16

Participant Flow

The IN.PACT SFA Trial was designed as a two-phase randomized trial. IN.PACT SFA I, the first phase was conducted in Europe with 150 subjects enrolled. IN.PACT SFA II, the second phase, was conducted in the US with 181 subjects enrolled. The data from both phases of the IN.PACT SFA Trial have been pooled and comprise the pivotal trial data.

Participant milestones

Participant milestones
Measure
Drug-Coated Balloon (DCB)
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm
Standard PTA
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm
IN.PACT SFA I Phase
STARTED
99
51
IN.PACT SFA I Phase
COMPLETED
88
49
IN.PACT SFA I Phase
NOT COMPLETED
11
2
IN.PACT SFA II Phase
STARTED
121
60
IN.PACT SFA II Phase
COMPLETED
109
55
IN.PACT SFA II Phase
NOT COMPLETED
12
5

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Randomized Trial of IN.PACT Admiral® Drug Coated Balloon vs Standard PTA for the Treatment of SFA and Proximal Popliteal Arterial Disease

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Drug-Coated Balloon (DCB)
n=220 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=111 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Total
n=331 Participants
Total of all reporting groups
Age, Continuous
67.5 Years
STANDARD_DEVIATION 9.5 • n=5 Participants
68.0 Years
STANDARD_DEVIATION 9.2 • n=7 Participants
67.5 Years
STANDARD_DEVIATION 9.4 • n=5 Participants
Sex: Female, Male
Female
77 Participants
n=5 Participants
36 Participants
n=7 Participants
113 Participants
n=5 Participants
Sex: Female, Male
Male
143 Participants
n=5 Participants
75 Participants
n=7 Participants
218 Participants
n=5 Participants

PRIMARY outcome

Timeframe: 12 Month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Primary patency is defined as freedom from clinically-driven target lesion revascularization (TLR) or restenosis as determined by duplex ultrasound (DUS) Peak Systolic Velocity Ratio (PSVR) ≤ 2.4.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=191 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=103 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Primary Patency
82.2 Percentage of participants
52.4 Percentage of participants

PRIMARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Primary safety composite is defined as freedom from death through 30 days or target limb major amputation or clinically-driven target vessel revascularization (CD-TVR) within 12 months post index procedure.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=207 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=107 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Primary Safety Composite
95.7 Percentage of Participants
76.6 Percentage of Participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Major Adverse Events (MAE) composite defined as all-cause death, clinically-driven target vessel revascularization (CD-TVR), major target limb amputation, thrombosis at the target lesion site

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=207 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=107 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Major Adverse Events (MAE) Composite
6.3 Percentage of participants
24.3 Percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=207 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=107 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
All-cause Death
1.9 percentage of participants
0.0 percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=207 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=107 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Target Vessel Revascularization (TVR)
4.8 Percentage of participants
23.4 Percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=207 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=107 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Target Lesion Revascularization (TLR)
2.9 Percentage of participants
20.6 Percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Includes all subjects who experienced a CD-TLR.

Clinically-driven target lesion revascularization (CD-TLR) is defined as any re-intervention within the target lesion due to symptoms or drop of ankle brachial index (ABI) of ≥20% or \>0.15 when compared to post-procedure baseline.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=5 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=22 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Time to First Clinically Driven Target Lesion Revascularization (CD-TLR)
144.6 Days
Standard Deviation 159.6
201.9 Days
Standard Deviation 90.9

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=207 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=107 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Major Target Limb Amputation
0 percentage of amputations
0 percentage of amputations

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=207 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=107 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Thrombosis at the Target Lesion
1.4 Percentage of participants
3.7 Percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Freedom from target limb amputation, target vessel revascularization (TVR), and increase in Rutherford class. Rutherford classification is a clinical staging system that is used to describe peripheral arterial disease.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=196 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=106 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Primary Sustained Clinical Improvement
85.2 percentage of particpants
68.9 percentage of particpants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Freedom from target limb amputation and increase in Rutherford class.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=196 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=104 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Secondary Sustained Clinical Improvement
89.3 percentage of participants
84.6 percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Duplex ultrasound measurement that measures the peak systolic velocity of blood (cm/sec) within a lesion divided by the peak velocity of blood (cm/sec) proximal to the lesion.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=188 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=86 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Duplex-defined Binary Restenosis (Peak Systolic Velocity Ratio (PSVR) >2.4).
16.5 Percentage of participants
33.7 Percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=178 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=84 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Duplex-defined Binary Restenosis (Peak Systolic Velocity Ratio >3.4).
7.3 Percentage of particpants
21.4 Percentage of particpants

SECONDARY outcome

Timeframe: Baseline to 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Quality of life assessment by EQ5D at 1 year compared to baseline. EQ5D is a standardised measure of health status and economic appraisal. The EQ5D consists of the EQ5D descriptive system which comprises the following variables for the 5 dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels: (1) no problems, (2) some problems, (3) extreme problems. A complex algorithm that took individual dimensions and generated an overall score was used. EQ5D health state is used in the algorithm to calculate an overall score where - 0.109 = 'worst possible outcome' and 1.000 = 'best possible outcome'.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=193 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=102 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Change From Baseline in Quality of Life Assessment by EuroQol Group 5-Dimension Self Report Questionnaire (EQ5D) at Month 12
0.1059 Units on a scale
Standard Deviation 0.2089
0.0730 Units on a scale
Standard Deviation 0.1951

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Walking capacity assessment by WIQ at 1 year compared to baseline. WIQ is a quality of life questionnaire that was specifically designed to assess the degree of impairment experienced by patients with claudication. Clinical outcomes were assessed by patients responses to question 1A. Question 1A is specific for calf or buttocks claudication and is used to create a summary score for analysis. Question 1A is expressed on a scale of 0% (unable to perform because of severe claudication) to 100% (no impairment).

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=196 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=104 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Change From Baseline in Walking Capacity Assessment by Walking Impairment Questionnaire (WIQ) at 12 Months
72.7 Units on a scale
Standard Deviation 31.4
73.6 Units on a scale
Standard Deviation 29.5

SECONDARY outcome

Timeframe: Day 1

Population: Total number of devices used in the ITT population (n=331).

Device success is defined as successful delivery, balloon inflation and deflation and retrieval of the intact study device without burst below rated burst pressure (RBP).

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=311 Devices
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=130 Devices
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Device Success
99.0 Percentage of devices
98.5 Percentage of devices

SECONDARY outcome

Timeframe: Day 1

Population: Intention-to-Treat (ITT) (n=331)

Procedural success is defined as obtainment of ≤30% residual stenosis by visual estimate (with or without stenting)

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=220 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=111 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Procedural Success
99.5 Percentage of participants
98.2 Percentage of participants

SECONDARY outcome

Timeframe: Day 1

Population: Intention-to-Treat (ITT) (n=331)

Clinical success is defined as procedural success without procedural complications (death, stroke, major target limb amputation, thrombosis of the target lesion, or target vessel revascularization (TVR)) prior to discharge.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=220 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=111 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Clinical Success
99.1 Percentage of participants
97.3 Percentage of participants

SECONDARY outcome

Timeframe: 12 month

Population: Intention-to-Treat (ITT) (n=331) that excludes subjects who did not have evaluable data at the reporting timeframe.

Days of hospitalization from procedure through 12 month.

Outcome measures

Outcome measures
Measure
Drug-Coated Balloon (DCB)
n=219 Participants
Paclitaxel drug-coated angioplasty balloon IN.PACT Admiral Drug-Coated Balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Standard PTA
n=111 Participants
Standard angioplasty balloon without Paclitaxel drug-coating Standard angioplasty balloon: Subjects will be randomized 2:1 to the IN.PACT Admiral Drug-Coated Balloon Arm or to the standard angioplasty balloon Arm.
Days of Hospitalization Due to the Index Lesion
1.3 Days
Standard Deviation 1.9
1.7 Days
Standard Deviation 2.0

Adverse Events

Drug-Coated Balloon (DCB)

Serious events: 102 serious events
Other events: 104 other events
Deaths: 0 deaths

Standard PTA

Serious events: 62 serious events
Other events: 62 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
Drug-Coated Balloon (DCB)
n=220 participants at risk
IN.PACT Admiral: Balloon Angioplasty Drug-Coated Balloon (DCB): balloon dilatation and provisional stenting with IN.PACT DCB
Standard PTA
n=111 participants at risk
Standard Percutaneous Transluminal Angioplasty (PTA) Balloon: Balloon Angioplasty PTA Balloon: Balloon Angioplasty: balloon dilatation and provisional stenting with standard non-coated PTA balloon
Gastrointestinal disorders
Abdominal Pain
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Acute Coronary Syndrome
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Acute Myocardial Infarction
1.4%
3/220 • Number of events 3
0.00%
0/111
Respiratory, thoracic and mediastinal disorders
Acute Pulmonary Oedema
0.45%
1/220 • Number of events 1
0.00%
0/111
General disorders
Adverse Drug Reaction
0.45%
1/220 • Number of events 1
0.00%
0/111
Nervous system disorders
Amnesia
0.45%
1/220 • Number of events 1
0.00%
0/111
Blood and lymphatic system disorders
Anaemia
1.8%
4/220 • Number of events 4
0.90%
1/111 • Number of events 1
Gastrointestinal disorders
MedDRA 13.0
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Angina Pectoris
0.91%
2/220 • Number of events 2
0.90%
1/111 • Number of events 1
Cardiac disorders
Angina Unstable
0.00%
0/220
0.90%
1/111 • Number of events 1
Vascular disorders
Aorto-Duodenal Fistula
0.00%
0/220
0.00%
0/111
Cardiac disorders
Arrhythmia
0.45%
1/220 • Number of events 2
0.00%
0/111
Vascular disorders
Arterial Occlusive Disease
0.45%
1/220 • Number of events 1
0.00%
0/111
Injury, poisoning and procedural complications
Arterial Restenosis
0.45%
1/220 • Number of events 1
3.6%
4/111 • Number of events 4
Vascular disorders
Arterial Stenosis Limb
0.45%
1/220 • Number of events 1
2.7%
3/111 • Number of events 3
Vascular disorders
Arterial Thrombosis Limb
0.00%
0/220
0.00%
0/111
Vascular disorders
Arteriovenous Fistula
0.00%
0/220
1.8%
2/111 • Number of events 2
Vascular disorders
Artery Dissection
3.2%
7/220 • Number of events 8
1.8%
2/111 • Number of events 2
Infections and infestations
Arthritis Bacterial
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Atrial Fibrillation
0.91%
2/220 • Number of events 2
1.8%
2/111 • Number of events 2
Musculoskeletal and connective tissue disorders
Back Pain
0.45%
1/220 • Number of events 1
0.90%
1/111 • Number of events 1
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Basal Cell Carcinoma
0.00%
0/220
0.90%
1/111 • Number of events 1
Hepatobiliary disorders
Bile Duct Obstruction
0.45%
1/220 • Number of events 1
0.00%
0/111
Infections and infestations
Biliary Sepsis
0.45%
1/220 • Number of events 1
0.00%
0/111
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Bladder Cancer
0.00%
0/220
0.90%
1/111 • Number of events 1
Infections and infestations
Bronchiectasis
0.00%
0/220
0.90%
1/111 • Number of events 1
Cardiac disorders
Cardiac Arrest
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Cardiac Failure Congestive
2.7%
6/220 • Number of events 6
0.90%
1/111 • Number of events 1
Nervous system disorders
Carotid Artery Disease
0.00%
0/220
0.90%
1/111 • Number of events 1
Nervous system disorders
Carotid Artery Stenosis
0.45%
1/220 • Number of events 1
1.8%
2/111 • Number of events 2
Infections and infestations
Cellulitis
0.00%
0/220
0.00%
0/111
Nervous system disorders
Cerebral Infarction
0.45%
1/220 • Number of events 1
0.90%
1/111 • Number of events 1
Nervous system disorders
Cerebrovascular Accident
0.45%
1/220 • Number of events 1
0.00%
0/111
General disorders
Chest Pain
0.91%
2/220 • Number of events 2
0.90%
1/111 • Number of events 1
Hepatobiliary disorders
Cholecystitis
0.45%
1/220 • Number of events 1
0.00%
0/111
Respiratory, thoracic and mediastinal disorders
Chronic Obstructive Pulmonary Disease
0.45%
1/220 • Number of events 1
0.00%
0/111
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Colon Cancer Metastatic
0.00%
0/220
0.90%
1/111 • Number of events 1
Cardiac disorders
Coronary Artery Disease
3.2%
7/220 • Number of events 7
0.90%
1/111 • Number of events 1
Cardiac disorders
Coronary Artery Thrombosis
0.00%
0/220
0.90%
1/111 • Number of events 1
General disorders
Device Occlusion
0.45%
1/220 • Number of events 1
0.90%
1/111 • Number of events 1
Infections and infestations
Device Related Infection
0.00%
0/220
0.00%
0/111
Metabolism and nutrition disorders
Diabetic Foot
0.00%
0/220
0.00%
0/111
Eye disorders
Diabetic Retinopathy
0.45%
1/220 • Number of events 1
0.00%
0/111
Skin and subcutaneous tissue disorders
Dry Gangrene
0.00%
0/220
0.90%
1/111 • Number of events 1
Respiratory, thoracic and mediastinal disorders
Dyspnoea Exertional
0.45%
1/220 • Number of events 1
0.00%
0/111
Nervous system disorders
Embolic Cerebral Infarction
0.45%
1/220 • Number of events 1
0.00%
0/111
Musculoskeletal and connective tissue disorders
Exostosis
0.45%
1/220 • Number of events 1
0.00%
0/111
Injury, poisoning and procedural complications
Facial Bones Fracture
0.45%
1/220 • Number of events 1
0.00%
0/111
Injury, poisoning and procedural complications
Fall
0.00%
0/220
0.90%
1/111 • Number of events 1
Vascular disorders
Femoral Arterial Stenosis
6.8%
15/220 • Number of events 18
9.0%
10/111 • Number of events 12
Vascular disorders
Femoral Artery Dissection
1.8%
4/220 • Number of events 4
4.5%
5/111 • Number of events 5
Vascular disorders
Femoral Artery Occlusion
1.4%
3/220 • Number of events 5
4.5%
5/111 • Number of events 5
Injury, poisoning and procedural complications
Femoral Neck Fracture
0.45%
1/220 • Number of events 1
0.90%
1/111 • Number of events 1
Injury, poisoning and procedural complications
Fibula Fracture
0.45%
1/220 • Number of events 1
0.00%
0/111
Injury, poisoning and procedural complications
Fractured Coccyx
0.45%
1/220 • Number of events 1
0.00%
0/111
Infections and infestations
Gangrene
0.91%
2/220 • Number of events 2
0.00%
0/111
Infections and infestations
Gastroenteritis
0.45%
1/220 • Number of events 1
0.00%
0/111
Gastrointestinal disorders
Gastrointestinal Haemorrhage
0.91%
2/220 • Number of events 2
0.90%
1/111 • Number of events 1
Gastrointestinal disorders
Gastrooesophageal Reflux Disease
0.45%
1/220 • Number of events 1
0.00%
0/111
Vascular disorders
Haematoma
0.00%
0/220
0.90%
1/111 • Number of events 1
Renal and urinary disorders
Haematuria
0.00%
0/220
0.90%
1/111 • Number of events 1
Vascular disorders
Haemorrhage
0.45%
1/220 • Number of events 1
0.00%
0/111
Nervous system disorders
Haemorrhage Intracranial
0.45%
1/220 • Number of events 1
0.00%
0/111
Blood and lymphatic system disorders
Haemorrhagic Anaemia
0.45%
1/220 • Number of events 1
0.00%
0/111
Hepatobiliary disorders
Hepatic Cirrhosis
0.00%
0/220
0.90%
1/111 • Number of events 1
Metabolism and nutrition disorders
Hyperglycaemia
0.45%
1/220 • Number of events 1
0.00%
0/111
Metabolism and nutrition disorders
Hyperkalaemia
0.45%
1/220 • Number of events 1
0.00%
0/111
Nervous system disorders
Hypoaesthesia
0.45%
1/220 • Number of events 1
0.00%
0/111
Vascular disorders
Hypotension
0.45%
1/220 • Number of events 1
0.00%
0/111
Vascular disorders
Iliac Artery Occlusion
0.00%
0/220
0.00%
0/111
Vascular disorders
Iliac Artery Stenosis
0.91%
2/220 • Number of events 2
0.90%
1/111 • Number of events 1
Gastrointestinal disorders
Impaired Gastric Emptying
0.45%
1/220 • Number of events 1
0.00%
0/111
General disorders
Impaired Healing
0.45%
1/220 • Number of events 2
0.90%
1/111 • Number of events 1
General disorders
Implant Site Thrombosis
0.45%
1/220 • Number of events 1
0.00%
0/111
Injury, poisoning and procedural complications
In-Stent Arterial Restenosis
1.4%
3/220 • Number of events 3
0.90%
1/111 • Number of events 1
Injury, poisoning and procedural complications
In-Stent Coronary Artery Restenosis
0.45%
1/220 • Number of events 1
0.00%
0/111
Infections and infestations
Infected Lymphocele
0.45%
1/220 • Number of events 1
0.00%
0/111
Vascular disorders
Intermittent Claudication
3.2%
7/220 • Number of events 7
9.9%
11/111 • Number of events 12
Musculoskeletal and connective tissue disorders
Intervertebral Disc Protrusion
0.00%
0/220
0.90%
1/111 • Number of events 1
Gastrointestinal disorders
Intestinal Obstruction
0.45%
1/220 • Number of events 1
0.00%
0/111
Surgical and medical procedures
Joint Surgery
0.45%
1/220 • Number of events 1
0.00%
0/111
Gastrointestinal disorders
Large Intestine Perforation
0.45%
1/220 • Number of events 1
0.00%
0/111
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Lipoma
0.00%
0/220
0.90%
1/111 • Number of events 1
Hepatobiliary disorders
Liver Disorder
0.45%
1/220 • Number of events 1
0.00%
0/111
Infections and infestations
Localised Infection
0.45%
1/220 • Number of events 1
0.00%
0/111
Nervous system disorders
Lumbar Radiculopathy
0.45%
1/220 • Number of events 1
0.00%
0/111
Musculoskeletal and connective tissue disorders
Lumbar Spinal Stenosis
0.91%
2/220 • Number of events 2
0.90%
1/111 • Number of events 1
Injury, poisoning and procedural complications
Lumbar Vertebral Fracture
0.45%
1/220 • Number of events 1
0.00%
0/111
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Malignant Melanoma
0.00%
0/220
0.00%
0/111
General disorders
Mass
0.00%
0/220
0.90%
1/111 • Number of events 1
Gastrointestinal disorders
Melaena
0.00%
0/220
0.90%
1/111 • Number of events 1
Psychiatric disorders
Mental Status Changes
0.00%
0/220
0.00%
0/111
General disorders
Multi-Organ Failure
0.45%
1/220 • Number of events 1
0.00%
0/111
Musculoskeletal and connective tissue disorders
Musculoskeletal Pain
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Myocardial Infarction
0.91%
2/220 • Number of events 2
0.90%
1/111 • Number of events 1
Cardiac disorders
Myocardial Ischaemia
0.45%
1/220 • Number of events 1
0.00%
0/111
General disorders
Necrosis
0.00%
0/220
0.90%
1/111 • Number of events 1
Skin and subcutaneous tissue disorders
Neuropathic Ulcer
0.00%
0/220
0.90%
1/111 • Number of events 1
Metabolism and nutrition disorders
Obesity
0.45%
1/220 • Number of events 1
0.00%
0/111
General disorders
Oedema Peripheral
0.45%
1/220 • Number of events 1
0.00%
0/111
Vascular disorders
Orthostatic Hypotension
0.45%
1/220 • Number of events 1
0.90%
1/111 • Number of events 1
Musculoskeletal and connective tissue disorders
Osteoarthritis
0.91%
2/220 • Number of events 2
0.00%
0/111
Infections and infestations
Osteomyelitis
0.00%
0/220
0.90%
1/111 • Number of events 1
Injury, poisoning and procedural complications
Overdose
0.00%
0/220
0.00%
0/111
Musculoskeletal and connective tissue disorders
Pain In Extremity
0.91%
2/220 • Number of events 2
0.90%
1/111 • Number of events 1
Gastrointestinal disorders
Pancreatitis
0.45%
1/220 • Number of events 2
0.00%
0/111
Blood and lymphatic system disorders
Pancytopenia
0.00%
0/220
0.90%
1/111 • Number of events 1
Nervous system disorders
Paraesthesia
0.00%
0/220
0.90%
1/111 • Number of events 1
Gastrointestinal disorders
Peptic Ulcer
0.00%
0/220
0.00%
0/111
Vascular disorders
Peripheral Arterial Occlusive Disease
3.6%
8/220 • Number of events 8
4.5%
5/111 • Number of events 5
Injury, poisoning and procedural complications
Peripheral Arterial Reocclusion
0.00%
0/220
3.6%
4/111 • Number of events 4
Vascular disorders
Peripheral Artery Dissection
1.4%
3/220 • Number of events 3
3.6%
4/111 • Number of events 5
Vascular disorders
Peripheral Embolism
0.45%
1/220 • Number of events 1
0.90%
1/111 • Number of events 1
Vascular disorders
Peripheral Ischaemia
0.91%
2/220 • Number of events 4
1.8%
2/111 • Number of events 2
Surgical and medical procedures
Peripheral Revascularisation
0.00%
0/220
0.90%
1/111 • Number of events 1
Vascular disorders
Peripheral Vascular Disorder
0.91%
2/220 • Number of events 2
0.00%
0/111
Gastrointestinal disorders
Peritonitis
0.45%
1/220 • Number of events 1
0.00%
0/111
Infections and infestations
Pneumonia
0.45%
1/220 • Number of events 1
0.00%
0/111
General disorders
Polyp
0.45%
1/220 • Number of events 1
0.00%
0/111
Reproductive system and breast disorders
Postmenopausal Haemorrhage
0.45%
1/220 • Number of events 1
0.00%
0/111
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Prostate Cancer
0.45%
1/220 • Number of events 1
0.00%
0/111
Investigations
Prostatic Specific Antigen Increased
0.00%
0/220
0.90%
1/111 • Number of events 1
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Renal Cancer
0.00%
0/220
0.90%
1/111 • Number of events 1
Renal and urinary disorders
Renal Colic
0.00%
0/220
0.90%
1/111 • Number of events 1
Renal and urinary disorders
Renal Failure
0.00%
0/220
0.90%
1/111 • Number of events 1
Renal and urinary disorders
Renal Failure Acute
0.45%
1/220 • Number of events 1
0.00%
0/111
Respiratory, thoracic and mediastinal disorders
Respiratory Failure
0.45%
1/220 • Number of events 1
0.90%
1/111 • Number of events 1
Infections and infestations
Sepsis
0.45%
1/220 • Number of events 1
0.00%
0/111
Vascular disorders
Shock Haemorrhagic
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Sinus Tachycardia
0.45%
1/220 • Number of events 1
0.00%
0/111
Gastrointestinal disorders
Small Intestinal Obstruction
0.45%
1/220 • Number of events 1
0.00%
0/111
Musculoskeletal and connective tissue disorders
Spinal Column Stenosis
0.00%
0/220
0.90%
1/111 • Number of events 1
Musculoskeletal and connective tissue disorders
Spinal Osteoarthritis
0.45%
1/220 • Number of events 1
0.00%
0/111
Musculoskeletal and connective tissue disorders
Spondylolisthesis
0.45%
1/220 • Number of events 1
0.00%
0/111
Vascular disorders
Subclavian Artery Stenosis
0.00%
0/220
0.90%
1/111 • Number of events 1
General disorders
Sudden Death
0.45%
1/220 • Number of events 1
0.00%
0/111
Cardiac disorders
Supraventricular Tachycardia
0.00%
0/220
0.90%
1/111 • Number of events 1
Nervous system disorders
Syncope
0.45%
1/220 • Number of events 1
1.8%
2/111 • Number of events 2
Musculoskeletal and connective tissue disorders
Synovial Cyst
0.45%
1/220 • Number of events 1
0.00%
0/111
Surgical and medical procedures
Therapeutic Embolisation
0.45%
1/220 • Number of events 1
0.00%
0/111
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Tonsil Cancer
0.45%
1/220 • Number of events 1
0.00%
0/111
Nervous system disorders
Transient Ischaemic Attack
1.4%
3/220 • Number of events 3
0.00%
0/111
Infections and infestations
Urinary Tract Infection
0.45%
1/220 • Number of events 1
0.00%
0/111
Injury, poisoning and procedural complications
Vascular Graft Occlusion
0.45%
1/220 • Number of events 2
0.00%
0/111
Injury, poisoning and procedural complications
Vascular Pseudoaneurysm
1.4%
3/220 • Number of events 3
2.7%
3/111 • Number of events 3
Cardiac disorders
Ventricular Tachycardia
0.45%
1/220 • Number of events 1
0.00%
0/111
Ear and labyrinth disorders
Vertigo
0.45%
1/220 • Number of events 1
0.00%
0/111
General disorders
Vessel Puncture Site Haematoma
0.91%
2/220 • Number of events 2
0.00%
0/111
Infections and infestations
West Nile Viral Infection
0.45%
1/220 • Number of events 1
0.00%
0/111

Other adverse events

Other adverse events
Measure
Drug-Coated Balloon (DCB)
n=220 participants at risk
IN.PACT Admiral: Balloon Angioplasty Drug-Coated Balloon (DCB): balloon dilatation and provisional stenting with IN.PACT DCB
Standard PTA
n=111 participants at risk
Standard Percutaneous Transluminal Angioplasty (PTA) Balloon: Balloon Angioplasty PTA Balloon: Balloon Angioplasty: balloon dilatation and provisional stenting with standard non-coated PTA balloon
Vascular disorders
Artery Dissection
20.9%
46/220 • Number of events 46
32.4%
36/111 • Number of events 37
Vascular disorders
Femoral Artery Dissection
13.2%
29/220 • Number of events 29
9.9%
11/111 • Number of events 11
Vascular disorders
Intermittent Claudication
0.00%
0/220
13.5%
15/111 • Number of events 16
Musculoskeletal and connective tissue disorders
Pain In Extremity
9.5%
21/220 • Number of events 23
7.2%
8/111 • Number of events 8
Vascular disorders
Peripheral Artery Dissection
6.4%
14/220 • Number of events 14
8.1%
9/111 • Number of events 11
General disorders
Vessel Puncture Site Haematoma
5.9%
13/220 • Number of events 13
0.00%
0/111

Additional Information

Clinical Research Director

Medtronic - CardioVascular

Phone: +31433566580

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place

Restriction type: GT60