Trials / Terminated
TerminatedNCT03346577
Endovascular Treatment of Peripheral Artery Disease
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (actual)
- Sponsor
- be Medical · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this observational study is to evaluate the performance and safety of endovascular treatment with stenting (Optimed Sinus Superflex 635) or balloon angioplasty (Cardionovum Legflow or Optimed Nylotrack .035 + .018) according to current practice. The goal of the study will be achieved by assessing binary restenosis with duplex ultrasound, peri- and postoperative complications, technical success, target lesion revascularization, amputation and clinical outcome.
Conditions
- Peripheral Arterial Disease
- Iliac Artery Disease
- Below-the-knee Obstruction
- Femoropopliteal Occlusive Disease
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | stent or balloon | Endovascular treatment with stent or balloon according to current practice |
Timeline
- Start date
- 2018-05-02
- Primary completion
- 2020-10-01
- Completion
- 2020-10-01
- First posted
- 2017-11-17
- Last updated
- 2021-01-14
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT03346577. Inclusion in this directory is not an endorsement.