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Clinical Trial

XPAD European Feasibility Study

NCT: NCT07716020 · NOT_YET_RECRUITING

NCT IDNCT07716020
StatusNOT_YET_RECRUITING
SponsorXeltis (INDUSTRY)
First posted
Last updated

Brief Summary

A prospective, single arm, non-randomized European feasibility study to evaluate the safety and performance of the XPAD conduit in patients with peripheral arterial occlusive disease (PAOD), scheduled to undergo elective lower-limb, above or below the knee, bypass surgery.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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