REFLOW Study, Investigating the Efficacy of the LEGFLOW DCB in TASC C&D Fempop Lesions

NCT ID: NCT02580955

Last Updated: 2018-08-13

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE3
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-10-31
• Study Completion Date: 2019-01-31

Brief Summary

A physician initiated trial investigating the LEGFLOW Paclitaxel-Eluting Peripheral Balloon dilatation catheter for the treatment of femoropopliteal lesions longer than 15cm.

Objective: to evaluate the short-term outcome of the treatment by means of the LEGFLOW Paclitaxel-Eluting Peripheral BAlloon Dilattaion for the treatment of long femoropopliteal lesions (TASC C&D).

Conditions

Peripheral Arterial Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

LEGFLOW DCB

patients treated with the LEGFLOW Paclitaxel-Eluting Peripheral Balloon Dilatation Catheter

Group Type: EXPERIMENTAL

LEGFLOW DCB

Intervention Type: DEVICE

Interventions

LEGFLOW DCB

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Patient presenting a score from 2 to 5 following Rutherford classification

2. Patient is willing to comply with specified follow-up evaluations at the specified times

3. Patient is >18 years old

4. Patient understands the nature of the procedure and provides written informed consent, prior to enrolment in the study

5. Patient has a projected life expectancy of at least 12 months

6. Prior to enrolment, the guidewire has crossed target lesion

7. Patient is eligible for treatment with the LEGFLOW Paclitaxel-Eluting Peripheral Balloon Dilatation Catheter

8. Male, infertile female or female of child bearing potential practicing an acceptable method of birth control with a negative pregnancy test within 7 days prior to study procedure

9. De novo lesion located in the femoropopliteal arteries suitable for endovascular therapy

10. The target lesion is located within the native femoropopliteal artery

11. The length of the target lesion is > 150mm and considered as TASC C or D lesion according to the TASC II classification.

12. The target lesion has angiographic evidence of stenosis > 50% or occlusion which can be passed with standard guidewire manipulation

13. Target vessel diameter visually estimated is >4mm and <6.5 mm

14. There is angiographic evidence of at least one-vessel-runoff to the foot, irrespective of whether or not outflow was re-established by means of previous endovascular intervention

Exclusion Criteria

1. Patient refusing treatment

2. Presence of a stent in the target lesion that was placed during a previous procedure

3. Untreated flow-limiting inflow lesions

4. Any previous surgery in the target vessel (including prior ipsilateral crural bypass)

5. Presence of an aortic thrombosis or significant common femoral ipsilateral stenosis

6. Previous bypass surgery in the same limb

7. Patients for whom antiplatelet therapy, anticoagulants or thrombolytic drugs are contraindicated

8. Patients who exhibit persistent acute intraluminal thrombus of the proposed lesion site

9. Perforation at the angioplasty site evidenced by extravasation of contrast medium

10. Patients with known hypersensitivity to heparin, including those patients who have had a previous incidence of heparin-induced thrombocytopenia (HIT) type II

11. Patients with uncorrected bleeding disorders

12. Aneurysm located at the level of the SFA

13. Non-atherosclerotic disease resulting in occlusion (e.g. embolism, Buerger's disease, vasculitis)

14. Severe medical comorbidities (untreated CAD/CHF, sever COPD, metastatic malignancy, dementia, etc.) or other medical condition that would preclude compliance with the study protocol or 1-year life expectancy

15. Major distal amputation (above the transmetatarsal) in the study limb or non-study limb

16. Septicemia or bacteremia

17. Ipsilateral iliac treatment before the target lesion procedure with a residual stenosis >30% or ipsilateral iliac treatment conducted after the target lesion procedure

18. Use of thrombectomy, atherectomy or laser devices during procedure

19. Any patient considered to be hemodynamically unstable at onset of procedure

20. Known allergy to contrast media that cannot be adequately pre-medicated prior to the study procedure

21. Patient is currently participating in another investigational drug or device study that has not completed the entire follow up period

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Flanders Medical Research Program

NETWORK

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

OLV Hospital

Aalst, , Belgium

Imelda Hospital Bonheiden

Bonheiden, , Belgium

AZ Sint-Blasius

Dendermonde, , Belgium

Heilig Hart Hospital

Tienen, , Belgium

Countries

Belgium

Other Identifiers

FMRP-150527

Identifier Type: -

Identifier Source: org_study_id