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