Achilles Non-SNIS REGENETEN
NCT: NCT07869121 · ENROLLING_BY_INVITATION
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Kurzzusammenfassung
The proposed study addresses this gap by prospectively evaluating patient-reported outcomes, imaging endpoints, and safety through 12 months after BCI-augmented repair in IAT and MSR patients. The purpose is to evaluate clinical outcomes (effectiveness) following the use of REGENETEN to augment Achilles tendon surgical procedures.
Offizielle Quelle
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