Prospective Randomized Blinded Trial of VersaWrap Tendon Protector for Zone 2 Flexor Tendon Injuries

Completed · Not applicable

Conditions studied: Flexor Tendon

In brief

To analyze outcomes between patients with Z2FT injuries following repair, randomized to two groups. The first group will be the negative control, with no tendon wrap. The second group will have a VersaWrap Tendon Protector applied over the site of the tendon repair. VersaWrap is current SOC at UF.

Key facts

Study ID

NCT04322370

Run by

University of Florida

People needed

11

Starts

2020-08-21

Expected to finish

2026-03-31

Last updated by the study team

2026-07-31

Who can join

Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adult patients presenting to the plastic surgery service with a zone 2 flexor tendon injury requiring surgical repair

You may not qualify if…

• Patients with a sensitivity or allergy to polysaccharides alginate, hyaluronic acid, or citrate
• Patients with psychiatric or medical problems that preclude them from having surgery
• Female patients that are pregnant or breastfeeding
• Prisoners
• Patients who are unwilling or unable to follow-up

Where it is running

• University of Florida — Gainesville, Florida, United States

Full record on ClinicalTrials.gov

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