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Clinical Trial 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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02942394
Study type Observational
Source Optimed Medizinische Instrumente GmbH
Contact
Status Completed
Phase
Start date December 2016
Completion date December 17, 2020

See also
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