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Novel endoscopic versus open carpal tunnel release for idiopathic carpal tunnel syndrome: a randomized controlled trial

Minimally invasive treatment of carpal tunnel syndrome: a study for novel endoscopic carpal tunnel release

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034411
Enrollment
Unknown
Registered
2020-07-04
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-03

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

Conditions

Carpal Tunnel Syndrome

Interventions

experimental group:Novel endoscopic carpal tunnel release
control group:conventional open carpal tunnel release surgery

Sponsors

Beijing Ji-Shui-Tan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Including criteria 1. Symptoms for at least 1 month in at least two digits on one hand that include thumb, index, long or radial side of ring finger 2. Failure for at least 1 month of non-surgical treatment (medicine, immobilization or local blocking) 3. Meet to the criteria of electromyography ; 4. Aged >= 18 years; 5. Willing to participate this trial; 6. Moderate or severe carpal tunnel syndrome according to Hamada classification. Electromyography criteria (any one of the following) 1. Median motor latency at the wrist >= 4.5ms; 2. Sensory conduction velocity of median nerve at the wrist <50m/s; 3. Abnormal appearance of an waveform of the abductor pollicis brevis muscle.

Exclusion criteria

Exclusion criteria: 1. Previous carpal tunnel surgery on the study hand; 2. Any wrist or hand surgery within the previous 6 months; 3. Moderate to severe arthritis involving the study hand or wrist; 4. Known tumor, mass, or deformity of the study hand or wrist; 5. History of severe trauma to the study hand or wrist; 6. Current pregnancy or lactation; 7. Evidence of diffuse peripheral neuropathy or cervical radiculopathy; 8. Cases who had labor compensation disputes; 9. The patients who were not suitable for endoscopic release due to anatomical variation or other factors.

Design outcomes

Primary

MeasureTime frame
Boston CTS questionnaire;

Secondary

MeasureTime frame
the time of patients recovered daility life and/or work;operative time and incision length;pain score;complication;DASH score;The Pittsburgh sleep quality index;

Countries

China

Contacts

Public ContactYaobin Yin

Beijing Ji-Shui-Tan Hospital

yinyaobin586@163.com+86 13466757558

Outcome results

None listed

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