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Prospective, Randomized, Controlled, Multicentre, Open Study Releas of Paclitaxel during PTA versus PTA alone for the treatment of de-novo occluded, stenotic or reoccluded, restenotic superficial femoral (SFA) or popliteal arteries.

Phase 4
Withdrawn
Conditions
narrowing of the bloodvessel
stenosis
10003216
Registration Number
NL-OMON35958
Lead Sponsor
Eurocor GmbH
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
Not specified
Target Recruitment
15
Inclusion Criteria

Patients with symptomatic ischemia, requiring treatment of SFA or popliteal artery

Exclusion Criteria

Pregnancy, aneurisma disease of the abdominal aorta, iliac or popliteal arteries, contraindication for anti platelet therapy, stroke<3months, prior surgery target lesion,

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Rate of clinically driven target lesion revascularization (TLR) at 6 months</p><br>
Secondary Outcome Measures
NameTimeMethod
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