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UnknownNCT01616888

Paclitaxel Eluting Balloon for SFA In-stent Restenosis

Rug Eluting Balloon With Paclitaxel for Treatment of In-stent Restenosis in Femoropopliteal Arteries

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
University Health Network, Toronto · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to evaluate the safety and efficacy on the use of drug eluting balloon (DEB) with paclitaxel to treat in-stent restenosis in femoropopliteal arteries.

Detailed description

Peripheral artery disease (PAD) in the lower extremities can cause claudication, pain in the legs or feet and slowly wounds that can affect patients' quality of life and increase the risk of leg amputation and death. Both conventional balloon angioplasty (CBA) alone and CBA plus bare metal stents are the current primary endovascular therapy to treat PAD. However, exaggerated neointimal hyperplasia leading to in-stent restenosis is associated with CBA. Paclitaxel coated balloons have been recognized to be safe and effective for the treatment of coronary in-stent restenosis, which the investigators hypothesize to be applicable in femoropopliteal cases.

Conditions

Interventions

TypeNameDescription
DEVICEPTA with drug eluting balloon with paclitaxelAngioplasty with drug eluting balloon with paclitaxel on femoropopliteal arteries

Timeline

Start date
2012-06-01
Primary completion
2015-06-01
Completion
2015-08-01
First posted
2012-06-12
Last updated
2014-12-09

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01616888. Inclusion in this directory is not an endorsement.

Paclitaxel Eluting Balloon for SFA In-stent Restenosis (NCT01616888) · Clinical Trials Directory