Comparing absorbable and non-absorbable sutures for carpal tunnel surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the incidence of wound infections in patients undergoing carpal tunnel release surgery using either absorbable or non-absorbable sutures. Carpal Tunnel Syndrome is a common condition that can lead to significant discomfort and loss of function, and surgical decompression is the most effective treatment. The study aims to determine if the type of suture material used affects the rate of post-surgical infections. The primary outcome will be measured using the ASEPSIS wound score, assessed by independent investigators, while patients will also report their pain levels during recovery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

• indication for carpal tunnel release

Exclusion Criteria:

* carpal tunnel syndrome which has yet been operated
* injection with corticosteroids

Where it's running

• Gelre Ziekenhuizen
  Apeldoorn, Netherlands Recruiting
• Deventer Ziekenhuis
  Deventer, Netherlands Recruiting

Study contacts

• Study coordinator: Pauline Verhaegen, MD PHD
• Email: paulineverhaegen@hotmail.com
• Phone: 0555811244

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Ultrasound-guided needle release plus dextrose (D5W) hydrodissection for carpal tunnel syndrome

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.