Does Addition of a Vessel Loop in Wound Closure Improve Suture Removal?

  • STATUS
    Recruiting
  • End date
    Dec 13, 2022
  • participants needed
    110
  • sponsor
    Carilion Clinic
Updated on 13 May 2021

Summary

This study will investigate whether adding a vessel loop under sutures after elective carpal tunnel release increases patient satisfaction with suture removal.

Description

Surgical wound closure with nonabsorbable stitches necessitates subsequent suture removal, a process that can be uncomfortable for the patient and consume clinic time and resources. Anecdotal evidence suggests that the addition of a vessel loop under the sutures both simplifies suture removal and reduces discomfort. In this study, we propose a prospective, randomized, controlled, superiority trial to assess the impact of a vessel loop wound closure and suture removal for elective carpal tunnel release (CTR). Patients will be prospectively enrolled to one of two groups: closure without a vessel loop or closure with a vessel loop. The primary outcome measure will be patient satisfaction with suture removal. Time for wound closure, time for suture removal, pain with suture removal and other patient reported outcomes will be measured. These data will allow us to determine the benefit of addition of a vessel loop in wound closure.

Details
Condition Client satisfaction, Suture, Complication, Suture, Complication, Suture, Complication, Suture, Complication
Treatment Vessel loop (FDA product code FZZ)
Clinical Study IdentifierNCT04339439
SponsorCarilion Clinic
Last Modified on13 May 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Patients undergoing elective primary CTR (CPT 64721) at Carilion Clinic for carpal tunnel syndrome (CTS) diagnosed by CTS-6 or electrodiagnostic studies (EDS)

Exclusion Criteria

Emergency procedures
Revision procedures
Bilateral procedures
Concomitant procedures
Inability to provide informed consent for the study
Non-native English speakers
Allergy to suture material
History of wrist trauma
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