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NCT07230782
Ultrasound-Guided Percutaneous Release vs. Open Surgery for Carpal Tunnel Syndrome
NA trial testing Percutaneous Ultrasound Guided Release of the Transverse Carpal Ligament in Carpal Tunnel Syndrome (CTS) in 200 participants. Completed in 1 February 2025.
20 January 2024
Quick facts
| Lead sponsor | Fundacin Biomedica Galicia Sur |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 200 |
| Start date | 10 January 2021 |
| Primary completion | 20 January 2024 |
| Estimated completion | 1 February 2025 |
| Sites | 1 location across Spain |
Drugs / interventions tested
- Percutaneous Ultrasound Guided Release of the Transverse Carpal Ligament
- Open release surgery
Conditions studied
- Carpal Tunnel Syndrome (CTS) — all drugs for Carpal Tunnel Syndrome (CTS) →
Sponsor
Fundacin Biomedica Galicia Sur — full company profile →
Who can join
18 and older, any sex, with Carpal Tunnel Syndrome (CTS). Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to compare the clinical and functional outcomes of two surgical approaches for the treatment of carpal tunnel syndrome (CTS): ultrasound-guided percutaneous release of the flexor retinaculum and conventional open surgery. The study population includes adults diagnosed with carpal tunnel syndrome who are candidates for surgical treatment. The main questions this study aims to answer are: Does ultrasound-guided percutaneous flexor retinaculum release provide superior short-term functional outcomes compared with conventional open surgery? Does the minimally invasive approach lead to faster symptom relief and postoperative recovery? Researchers will compare the percutaneous ultrasound-guided technique with the traditional open palmar incision to determine whether the minimally invasive method offers measurable clinical advantages. Participants will: Undergo either ultrasound-guided percutaneous release or standard open surgical release, depending on group allocation. Complete validated clinical and functional assessments at predefined postoperative time points. Report symptom severity, functional status, and any procedure-related adverse events.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07230782
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Fundacin Biomedica Galicia Sur trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT07230782 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Fundacin Biomedica Galicia Sur
- Last refreshed: 17 November 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07230782.
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