Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DEVICE | PTA with drug eluting balloon with paclitaxel | Angioplasty 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.