Prospective Randomized Blinded Trial of VersaWrap Tendon Protector for Zone 2 Flexor Tendon Injuries
Recruiting
N/A
Interventional Study
Flexor Tendon
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 99
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 42 (estimated)
- Sponsor
- University of Florida · Other
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About This Trial
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.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adult patients presenting to the plastic surgery service with a zone 2 flexor tendon injury requiring surgical repair
Exclusion Criteria:
* Patients with a sensitivity or allergy to polysaccharides alginate, hyaluronic acid, or citrate
* Patients with psychiatric or medic…
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