Comparing absorbable and non-absorbable sutures for carpal tunnel surgery
Absorbable Versus Non-absorbable Sutures for Wound Closure in Carpal Tunnel Release: a Randomized Controlled Trial
This study is testing whether using absorbable or non-absorbable stitches during carpal tunnel surgery affects the chances of getting an infection afterward.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 2604 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Gelre Hospitals Academic / other |
| Locations | 2 sites (Apeldoorn and 1 other locations) |
| Trial ID | NCT05431101 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals scheduled for carpal tunnel release surgery.
Not a fit: Patients who have previously undergone carpal tunnel surgery or have received corticosteroid injections for their condition may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could help identify the optimal suture type to reduce the risk of wound infections after carpal tunnel surgery.
How similar studies have performed: While there is ongoing debate in the literature regarding the superiority of absorbable versus non-absorbable sutures, this study aims to provide clearer evidence on the topic.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: • indication for carpal tunnel release Exclusion Criteria: * carpal tunnel syndrome which has yet been operated * injection with corticosteroids
Where this trial is running
Apeldoorn and 1 other locations
- Gelre Ziekenhuizen — Apeldoorn, Netherlands (Recruiting)
- Deventer Ziekenhuis — Deventer, Netherlands (Recruiting)
Study contacts
- Study coordinator: Pauline Verhaegen, MD PHD
- Email: paulineverhaegen@hotmail.com
- Phone: 0555811244
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.