Trials / Completed
CompletedNCT02942394
Treatment of the Postthrombotic Syndrome With the Oblique Stent - TOPOS Study
Non-interventional, Multicenter, Multinational Venous Stent Study for the Treatment of the Post-thrombotic Syndrome With Common Iliac Vein Compression
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (actual)
- Sponsor
- Optimed Medizinische Instrumente GmbH · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Primary objective: To assess the efficacy of the stents (sinus-Obliquus stent for the common iliac vein, the sinus-XL Flex stent or sinus-Venous stent for the external iliac and common femoral veins) by evaluating different gradations of patency rates, patient's rating of disease severity and quality of life in patients with post-thrombotic syndrome and concomitant common iliac vein compression. Secondary objective: To assess long-term safety of venous stenting
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | sinus-Obliquus Stent System |
Timeline
- Start date
- 2016-12-01
- Primary completion
- 2020-12-17
- Completion
- 2020-12-17
- First posted
- 2016-10-24
- Last updated
- 2021-01-12
Locations
7 sites across 4 countries: Austria, Germany, Netherlands, Switzerland
Source: ClinicalTrials.gov record NCT02942394. Inclusion in this directory is not an endorsement.