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A comparative study on the efficacy and safety of ultrasound-guided acupotomy release versus mini-open carpal tunnel release in the treatment of carpal tunnel syndrome

A comparative study on the efficacy and safety of ultrasound-guided acupotomy release versus mini-open carpal tunnel release in the treatment of carpal tunnel syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116601
Enrollment
Unknown
Registered
2026-01-13
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome

Interventions

Ultrasound-guided needle-knife release group:Perform ultrasound-guided needle-knife release
Mini-open carpal tunnel release group:Perform mini-open carpal tunnel release

Sponsors

Northern Jiangsu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) 18 to 70 years old; (2) patients with typical symptoms of CTS (numbness, tingling, weakness, aggravation of symptoms at night) and typical signs (positive Tinel sign or Phalen sign of median nerve); (3) Electromyography showed median nerve damage; (4) B-ultrasound examination showed median nerve compression in the carpal tunnel; (5) Conservative treatment such as oral mecobalamin and local injection of corticosteroids is not effective; (6) able to understand the study process, voluntarily participate in this study, accept postoperative follow-up, and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) B-ultrasound examination showed median nerve bifurcation, persistent median artery, or carpal tunnel compression caused by tumor or fracture block at the entrance of carpal tunnel. (2) systemic or surgical site infection; (3) cervical spondylotic radiculopathy or diabetic peripheral neuropathy; (4) allergy to local anesthetic drugs; (5) Unable to complete the questionnaire due to language and cognitive impairment; (6) pregnant or lactating; (7) patients with severe heart disease and uncontrolled hypertension are expected to be unable to tolerate surgery; (8) There are any conditions that may affect the study participation or the safety of the subjects in the judgment of the investigator, such as concomitant diseases, mental disorders, uncontrolled infections, etc.

Design outcomes

Primary

MeasureTime frame
Cross-sectional area of the median nerve at the hamate plane compression;Cross-sectional area of the median nerve at the carpal tunnel entrance;Cross-sectional area of the median nerve at the exit of the carpal tunnel;Boston carpal tunnel questionnaire symptom severity scale scores;Boston carpal tunnel syndrome questionnaire functional status scale;Visual analogue scale scores;

Secondary

MeasureTime frame
Electrophysiological indicators;Cost of surgery;

Countries

China

Contacts

Public ContactXiaoqin Qian

Northern Jiangsu People's Hospital

yz_tyz1030@126.com+86 138 1318 6750

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026