Balloon Angioplasty Versus Primary Stenting for the Treatment of Femoropopliteal Artery Chronic Total Occlusions

NCT ID: NCT01268722

Last Updated: 2012-04-06

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 150 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-12-31
• Study Completion Date: 2016-12-31

Brief Summary

This is a multicenter double-arm randomized trial investigating plain balloon angioplasty versus primary placement of self-expanding nitinol stents after endovascular recanalization of femoral CTOs. Study will recruit up to 200 patients to be adequately powered for detection of a significant difference in vessel patency after 1 year.

Detailed Description

Primary placement of new-generation nitinol stents compared to plain old balloon angioplasty has shown encouraging long-term results in the femoropopliteal artery. However, there is complete lack of data about performance of new-generation nitinol stents in the treatment of chronic total occlusions (CTO) of the Femoral artery. This is a multicenter double-arm randomized trial investigating plain balloon angioplasty versus primary placement of self-expanding nitinol stents after endovascular recanalization of femoral CTOs. Study will recruit up to 200 patients to be adequately powered for detection of a significant difference in vessel patency after 1 year.

Conditions

Chronic Total Occlusion of Artery of the Extremities

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Balloon

Group Type: ACTIVE_COMPARATOR

Balloon angioplasty

Intervention Type: DEVICE

This arm will include patients randomized to undergo the treatment of a chronic total occlusion of the femoropopliteal artery with the use of balloon angioplasty

Stent

Group Type: EXPERIMENTAL

Primary stenting

Intervention Type: DEVICE

This arm will include patients randomized to undergo primary stenting of the femoropopliteal chronic total occlusion

Interventions

Balloon angioplasty

This arm will include patients randomized to undergo the treatment of a chronic total occlusion of the femoropopliteal artery with the use of balloon angioplasty

Intervention Type: DEVICE

Primary stenting

This arm will include patients randomized to undergo primary stenting of the femoropopliteal chronic total occlusion

Intervention Type: DEVICE

Other Intervention Names

Percutaneous angioplasty; Balloon dilatation; Self-expandable; Nitinol stents

Eligibility Criteria

Inclusion Criteria

• Age >/= 30 years, both genders, no healthy volunteers
• Negative pregnancy test for women of childbearing age
• Symptomatic leg ischemia by Rutherford/Becker Classification (category 3, 4 or 5), i.e. lifestyle-limiting claudication or critical limb ischemia Single completely occluded de-novo superficial femoral artery lesion (femoral artery CTO target lesion)
• Combined overall length of treatable occluded SFA lesion >/= 4.0 cm to </= 15.0 cm, by visual estimate. The occlusion must be treatable with no more than two stents, minimizing the stent overlap.
• Randomization process before successful subintimal or intraluminal recanalization of the lesion in order to evaluate technical success
• Use of re-entry devices at the discretion of the operator
• All lesions are to be located at least three centimeters (3 cm) proximal to the superior edge of the patella
• Reference vessel diameter (RVD) >/= 4.0 mm and </ 6.0 mm by visual assessment
• At least 1 patent infrapopliteal and popliteal artery, i.e., single vessel runoff or better with at least one of three vessels patent (< 50% stenosis) to the ankle or foot
• Poor aortoiliac or common femoral "inflow" (i.e. angiographically defined > 50% stenosis of the iliac or common femoral artery) lesions must be successfully treated prior to treatment of the target lesion
• Bilateral obstructive SFA disease is eligible for enrollment into the study
• Patient or authorized representative must provide written informed consent prior to initiation of study procedures
• Patient must be willing to comply with the specified follow-up protocol

Exclusion Criteria

• In-stent restenotic lesions (ISR occlusions)
• Distal popliteal of 3-vessel tibial occlusion
• Patients on hemodialysis because of heavily calcified vessels
• Recent thrombophlebitis, uremia, or deep venous thrombus (within past 30 days)
• Patients receiving dialysis or immunosuppressant therapy
• Thrombolysis of the target vessel within 72 hours prior to the index procedure with residual intraluminal thrombi
• Recent major stroke within the past 6 months
• Aneurysmal disease of the aorta, iliac, femoral or popliteal arteries
• Required stent placement across or within 0.5 cm of the femoral bifurcation
• Significant vessel tortuosity or other parameters prohibiting access to the lesion or 90° tortuosity which would prevent delivery of a stent device if necessary
• Known allergies to the following: aspirin, clopidogrel bisulfate (Plavix®) or ticlopidine (Ticlid®), heparin, Nitinol (nickel titanium), contrast agent, that cannot be medically managed
• Serum creatinine level >/= 2.5 mg/dl at time of screening visit
• Known or suspected active infection at the time of the procedure
• Bleeding diathesis
• Presence of an aortic, iliac or femoral artificial graft
• Life expectancy less than one year, or any other factors preventing clinical follow-up.
• Use of cryoplasty, laser, or atherectomy devices on the target vessel at the time of index procedure
• Patient is unwilling or unable to comply with procedures specified in the protocol or has difficulty or inability to return for follow-up visits as specified by the protocol
• Patient is known to be pregnant, incarcerated, mentally incompetent, and/or alcohol or drug abuser
• Patient is currently participating in any other investigational drug or medical device study that has not completed primary endpoint(s) evaluation or clinically interferes with the endpoints from this study or future participation in such studies prior to the completion of this study.
• Patient has had major surgical or interventional procedures unrelated to this study within 30 days prior to this study or planned surgical or interventional procedures within 30 days of entry into this study.

• Minimum Eligible Age: 30 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Patras

OTHER

Sponsor Role: lead

Responsible Party

SIABLIS DIMITRIOS

Professor of Radiology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Dimitrios Siablis, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital of Patras

Locations

Patras University Hospital

Rio, Achaia, Greece

Site Status: RECRUITING

Attikon University Hospital

Athens, Attica, Greece

Site Status: RECRUITING

Heraklion University Hospital

Heraklion, , Greece

Site Status: RECRUITING

Insubria University Hospital

Varese, Varese, Italy

Site Status: RECRUITING

Guy's and St Thomas' Hospitals, NHS Foundation Trust

London, , United Kingdom

Site Status: NOT_YET_RECRUITING

Countries

Greece; Italy; United Kingdom

Central Contacts

Dimitrios Siablis, MD, PhD

Role: CONTACT

siablis@upatras.gr

2613603219 ext. +30

Dimitrios Karnabatidis, MD, PhD

Role: CONTACT

karnaby@med.upatras.gr

2613603218 ext. +30

Facility Contacts

Dimitrios Siablis, MD,PhD

Role: primary

siablis@upatras.gr

2613603219 ext. +30

Dimitrios Karnabatidis, MD,PhD

Role: backup

karnaby@med.upatras.gr

2613603218 ext. +30

Elias Brountzos, MD,PhD

Role: primary

ebrountz@med.uoa.gr

2105831810 ext. +30

Dimitrios Tsetis, MD,PhD

Role: primary

tsetis@med.uoc.gr

Gianpaolo Carrafiello, MD,PhD

Role: primary

gianpaolo.carrafiello@unisubria.it

0332 278763 ext. +39

Tarun Sabharwal, FRCR

Role: primary

tarun_sabharwal@yahoo.co.uk

Other Identifiers

30357/2-12-2010

Identifier Type: -

Identifier Source: org_study_id