Outcomes for VersaWrap in Achilles Tendon Repair

Part of paid clinical trials in Sacramento, California.

Sponsor
Research Source
Study ID
NCT07025252
Status
Enrolling By Invitation

Conditions

  • Achilles Tendon Injury

Eligibility Criteria

Sex
ALL
Age
18 Years - 90 Years
Healthy Volunteers
Accepted

Interventions

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

Study Details

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

Key Dates

Start date
May 13, 2025
Status verified
Jun 2025
Primary completion
Jun 30, 2028
Completion
Jun 30, 2028

Study Design

Enrollment
400 participants (estimated)

Arms

  • Arm: VersaWrap
    All enrolled patients will received VersaWrap applied prior to surgical closure on the affected tendon.

Primary Outcome Measure

Skin Excursion [ Time Frame: 12 months post surgery ]

Locations (3)

FacilityCityStateZIPSite coordinators
UC Davis Foot and Ankle Orthopaedics ClinicSacramentoCalifornia95816-
Rothman Orthopaedics InstitutePhiladelphiaPennsylvania19107-
Medical University of South CarolinaCharlestonSouth Carolina29452-

Find similar trials in Sacramento, CA

By research site
UC Davis Foot and Ankle Orthopaedics Clinic· Sacramento, CARothman Orthopaedics Institute· Philadelphia, PAMedical University of South Carolina· Charleston, SC

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