A Single-center, Prospective, Clinical Study of VersaWrap Utilization in the Hand
Completed
Conditions studied: Tendon Repair, Fracture Repair, Tenolysis
In brief
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
Key facts
- Study ID
- NCT05598801
- Run by
- Research Source
- People needed
- 17
- Starts
- 2022-09-01
- Expected to finish
- 2025-08-17
- Last updated by the study team
- 2025-09-05
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Patients aged 18-70 at the time of surgery
- Patients undergoing hand/finger surgery, including tendon repair, fracture repair or tenolysis
- Psychosocially, mentally and physically able to fully comply with this protocol including adhering to follow-up schedule, study requirements with a signed informed consent with a study collaborator present at the time of signing to ensure compliance.
You may not qualify if…
- Non-English speaking
- Known allergy or sensitivity to citrate, alginate or hyaluronate
- Pregnant or breastfeeding
- Currently a prisoner
- Patient has any condition, that in the opinion of the Investigator, would prohibit the patient from complying with the protocol
Where it is running
- Austin Hand Group — Austin, Texas, United States
Full record on ClinicalTrials.gov
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