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PANACHE: A Pilot randomised trial comparing two forms of Absorbable versus Non-Absorbable sutures for Carpal tunnel Hand surgEry

Not Applicable
Conditions
Carpal tunnel release surgery in patients with carpal tunnel syndrome
Surgery
Registration Number
ISRCTN11774433
Lead Sponsor
Accord (United Kingdom)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
92
Inclusion Criteria

1. Any adult patient (18 years or older at the time of surgery)
2. Scheduled to undergo a primary CTR during the period of recruitment
3. CTR performed through a standard open approach procedure
4. Able and willing to give consent to surgical procedure and follow-up

Exclusion Criteria

1. Patient unable to provide informed consent
2. Revision/repeat carpal tunnel surgery
3. Adoption of a surgical approach different from the standard open incision (including extended carpal tunnel incision)
4. Additional simultaneous procedure(s) to the same upper limb
5. CTR performed in the context of trauma (non-elective procedure)
6. Patient did not receive the pre-enrolment information pack on the RCT prior to surgery
7. Patient non-English speaker
8. Patient unable to fill in questionnaires
9. Patient expresses a strong preference for one type of suture over the others when the option of different sutures is explained

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The proportion of randomised patients from those eligible and approached measured using the electronic screening log at the end of the 92-day recruitment window
Secondary Outcome Measures
NameTimeMethod
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