Wound Closure Study in Carpal Tunnel and Trigger Finger Surgery

Description

Does a difference in patient satisfaction and cosmetic outcome exist between wound closure with absorbable or non-absorbable sutures.

Conditions

Carpal Tunnel Syndrome, Trigger Finger

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Study Overview

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Study Details

Study overview

Does a difference in patient satisfaction and cosmetic outcome exist between wound closure with absorbable or non-absorbable sutures.

Absorbable Versus Non-Absorbable Suture in Carpal Tunnel and Trigger Finger Wound Closure

Wound Closure Study in Carpal Tunnel and Trigger Finger Surgery

Condition
Carpal Tunnel Syndrome
Intervention / Treatment

-

Contacts and Locations

Rochester

Mayo Clinic in Rochester, Rochester, Minnesota, United States, 55905

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Any patient greater than or equal to 18 years of age.
  • * Any patient undergoing primary open carpal tunnel release or primary trigger finger pulley release
  • * Any patient identified outside of the proposed study time period.
  • * Any patient receiving revision surgery
  • * Patients who have had prior ipsilateral palmar or finger surgery
  • * Patients with Dupuytren's disease

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Mayo Clinic,

Peter C Rhee, PRINCIPAL_INVESTIGATOR, Mayo Clinic

Study Record Dates

2026-01