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An Absorbable Suture Versus a Non-absorbable Suture in Carpal Tunnel Release, a Randomized Controlled Trial

Study acronym: SUPER
StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Primary completion date changed from estimate of May 31, 2024 to Nov 30, 2024
    • Trial status: Recruiting to Active, Not Recruiting
    • Study completion date: Aug 31, 2024 to Dec 2025
    • Site details revised
    v6
  2. Re-verified, no change to tracked fieldsv5
  3. Enrollment target: 144 to 116
    • Eligibility criteria expanded, about 23 words
    • Secondary endpoints: 3 to 6
    v4
  4. Re-verified, no change to tracked fieldsv3
  5. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Sep 2022 to Sep 21, 2022
    • Interventions: suture (Device) to Surgical wound closed with a non-absorbable suture (Procedure), Surgical wound closed with an absorbable suture (Procedure)
    • Site details revised
    v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The study compares two widely used treatments in closing the wound after open carpal tunnel release surgery: absorbable and non-absorbable sutures. It is conducted as a randomized controlled trial, where the participants are divided into two research groups. The visual outcome of the scar will be evaluated a year after the surgery.
Trial Details
NCT Number NCT05503719
Lead Sponsor Kuopio University Hospital
Collaborators: University of Eastern Finland
Conditions
(from sponsor)		 Carpal Tunnel Syndrome, Median Nerve Entrapment
Related terms Carpal Tunnel Syndrome, Median Neuropathy
Enrollment 116 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov