Trials / Withdrawn
WithdrawnNCT01667393
Popliteal Artery of Treatment With Balloon Angioplasty vs. SUPERA VERITAS Peripheral Stent System
Popliteal Artery Trial of Patients Undergoing Treatment With Balloon Angioplasty vs. the Adaptive SUPERA VERITAS Peripheral Stent System
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Abbott Medical Devices · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Unblinded, randomized, balanced trial comparing 12 month target lesion patency rates of the IDEV SUPERA VERITAS peripheral stent system to PTA in the treatment of obstructive atherosclerotic popliteal artery disease.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | IDEV SUPERA Stent | |
| DEVICE | Percutaneous Transluminal Angioplasty |
Timeline
- Start date
- 2013-01-01
- Primary completion
- 2013-01-01
- Completion
- 2013-01-01
- First posted
- 2012-08-17
- Last updated
- 2019-04-17
Source: ClinicalTrials.gov record NCT01667393. Inclusion in this directory is not an endorsement.