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Enrolling By Invitation NCT05598801

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

Conditions: Tendon Repair, Fracture Repair, Tenolysis

Sex: All
Ages: 18 Years – 70 Years
Healthy volunteers: 1
Enrollment: 20
Sponsor: Research Source

Location: United States

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

Eligibility Criteria

Inclusion Criteria:Patients aged 18-70 at the time of surgeryPatients undergoing hand/finger surgery, including tendon repair, fracture repair or tenolysisPsychosocially, 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.Exclusion Criteria:Non-English speakingKnown allergy or sensitivity to citrate, alginate or hyaluronatePregnant or breastfeedingCurrently a prisonerPatient has any condition, that in the opinion of the Investigator, would prohibit the patient from complying with the protocol

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05598801). StuddyBuddy aggregates publicly available trial information.