RecruitingNot ApplicableNCT05431101

abSorbable vErsus Non-absorbable SuturEs for Wound Closure in Carpal Tunnel Release

Absorbable Versus Non-absorbable Sutures for Wound Closure in Carpal Tunnel Release: a Randomized Controlled Trial


Sponsor

Gelre Hospitals

Enrollment

2,604 participants

Start Date

May 1, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Carpal Tunnel Syndrome is a prevalent condition, up to 9% in women and 0.6% in men. Surgical decompression in the most effective treatment. After surgery, approximately 1,8% of the patients develop a wound infection. Possibly, the type of sutures used can influence the prevalence of wound infection. In this RCT the incidence of infection is investigated between the use of absorbable versus non-absorbable sutures in carpal tunnel release.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Carpal Tunnel Release for people with suture, complication, wound infection, and other related conditions. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURECarpal Tunnel Release

Transection of flexor retinaculum for patients who have carpal tunnel syndrome


Locations(2)

Gelre Ziekenhuizen

Apeldoorn, Netherlands

Deventer Ziekenhuis

Deventer, Netherlands

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NCT05431101


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