Wound Closure Study in Carpal Tunnel and Trigger Finger Surgery

Withdrawn before enrolling · Not applicable

Conditions studied: Carpal Tunnel Syndrome, Trigger Finger

In brief

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

Key facts

Study ID

NCT03781141

Run by

Mayo Clinic

People needed

0

Starts

2019-12-01

Expected to finish

2026-03-01

Last updated by the study team

2026-03-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Mayo Clinic in Rochester — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

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