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Clinical efficiency observation of single incision and no special instrument assisted modified endoscopy release in treatment of carpal tunnel syndrome.

Comparison of clinical outcomes between open and modified endoscopic release for carpal tunnel syndrome

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041165
Enrollment
Unknown
Registered
2020-12-20
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-03-01

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

Conditions

carpal tunnel syndrome

Interventions

control group:traditional open release
experimental group:modified endoscopic release

Sponsors

Department of Orthopedics, Sir Run Run Hospital, Nanjing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: The following inclusion criteria were applied: 1) Typical symptoms (pain, hypesthesia or paresthesia) on one hand, including the thumb, index or middle finger; 2) The symptoms were unrelieved, recurrent and even aggravated after regular non-surgical treatment for > 3 months; 3) Hamada Grade I or II; 4) The presence of night pain that awoke the patients and a positive flick test (shaking the wrist when the patients were asked what they do to relieve symptoms) were required.

Exclusion criteria

Exclusion criteria: 1) Presence of secondary causes, such as bone abnormalities of the wrist, joint deformity or wrist occupations, including tumors or masses; 2) Diagnosis of inflammatory joint disease, trauma, diabetes mellitus or thyroid disorder to the affected hand during the preceding year, or pregnancy; 3) Previous CTR surgery in the affected hand or CTR surgery in the contralateral hand during the preceding year; 4) Inability to complete questionnaires; 5) Evidence of diffuse peripheral neuropathy or cervical radiculopathy.

Design outcomes

Primary

MeasureTime frame
operation time;average hospitalization time;the time needed to resume normal lifestyle and activity;incision infection rate;clinical symptoms amelioration (kelly);scar pain scor;two-point discrimination;incidence of sympathetic dystrophy;

Countries

China

Contacts

Public ContactJian Qin

Sir Run Run Hospital, Nanjing Medical University

qinjian@njmu.edu.cn+86 18351973783

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026