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Clinical Trial Summary

Prospective, non-randomized, multicenter pre-market feasibility study to evaluate subjects treated with the BlueLeaf System for the treatment of symptomatic CVI of the lower extremity.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05047302
Study type Interventional
Source Intervene, Inc.
Contact
Status Withdrawn
Phase N/A
Start date October 1, 2022
Completion date November 1, 2026

See also
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