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A Single-center, Prospective, Clinical Study of VersaWrap Utilization in the Hand

NCT05598801 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 17

Last updated 2025-09-05

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 hand/fingers, including tendon repair, fracture repair, or tenolysis of the hand/fingers. VersaWrap is designed to allow tendon gliding and to protect tendon gliding postoperatively

Conditions

  • Tendon Repair
  • Fracture Repair
  • Tenolysis

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
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-09-01
Primary Completion
2025-08-17
Completion
2025-08-17
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 NCT05598801 on ClinicalTrials.gov