Trials / Completed
CompletedNCT05598801
A Single-center, Prospective, Clinical Study of VersaWrap Utilization in the Hand
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 17 (actual)
- Sponsor
- Research Source · Network
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Accepted
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
Detailed description
This is a prospective, post-market, observational, single center study evaluating the use of VersaWrap. Patients identified by the Investigator in his practice as needing surgery of the hand/fingers and meeting all the inclusion and none of the exclusion. Patients will consent to participating in the study, prior to any study procedures.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | VersaWrap | VersaWrap is applied to the affected tendon to allow post-operative gliding. |
Timeline
- Start date
- 2022-09-01
- Primary completion
- 2025-08-17
- Completion
- 2025-08-17
- First posted
- 2022-10-28
- Last updated
- 2025-09-05
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05598801. Inclusion in this directory is not an endorsement.