Outcomes for VersaWrap in Achilles Tendon Repair

NCT07025252 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2025-06-17

No results posted yet for this study

Summary

The purpose of this study is to evaluate the efficacy on the use of VersaWrap® in surgery of the foot and ankle. VersaWrap is designed to allow tendon gliding and to protect tendon gliding postoperatively

Conditions

  • Achilles Tendon Injury

Interventions

DEVICE

VersaWrap

VersaWrap is applied to the affected tendon to allow post-operative gliding.

Sponsors & Collaborators

  • Research Source

    lead NETWORK

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-05-13
Primary Completion
2028-06-30
Completion
2028-06-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07025252 on ClinicalTrials.gov