Trials / Completed
CompletedNCT02522884
Tack Optimized Balloon Angioplasty Study of the Tack Endovascular System™ in Femoropoliteal Arteries
Tack Optimized Balloon Angioplasty Study for Superficial Femoral and Proximal Popliteal Arteries Using the Tack Endovascular System™
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 213 (actual)
- Sponsor
- Philips Clinical & Medical Affairs Global · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a prospective, multi-center, single-arm, non-blinded study designed to investigate the safety and efficacy of the Tack Endovascular System in subjects with post-balloon angioplasty (post-PTA) dissection(s) type(s) A through F in the superficial femoral and proximal popliteal arteries ranging in diameter from 2.5mm to 6.0mm.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Tack Endovascular System | Repair of post-PTA dissections using the Intact Vascular Tack Endovascular System. |
Timeline
- Start date
- 2015-09-01
- Primary completion
- 2018-05-01
- Completion
- 2020-03-01
- First posted
- 2015-08-13
- Last updated
- 2021-04-27
- Results posted
- 2019-12-10
Locations
39 sites across 3 countries: United States, Austria, Netherlands
Source: ClinicalTrials.gov record NCT02522884. Inclusion in this directory is not an endorsement.