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Electroacupuncture and Wrist Splinting for Carpal Tunnel Syndrome: A Randomized Trial in Primary Care Setting

Electroacupuncture and Wrist Splinting for Carpal Tunnel Syndrome: A Randomized Trial in Primary Care Setting

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001655
Enrollment
Unknown
Registered
2011-11-04
Start date
2012-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Carpal Tunnel Syndrome

Interventions

Two groups:Group 1: Night Splinting Plus Electroacupuncture”
Group 2: Night Splinting Plus Waiting List. Access the partner registry to get the detail discription. Duration: 17 weeks

Sponsors

JC School of Public Health and Primary Care, The Chinese University of Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients aged 18-70 and fulfilling the Katz CTS hand diagram criteria of (1) Classic / Probable Symptoms or (2) Possible Symptoms. Eligible patients should also (3) have the ability to read and speak Chinese (Cantonese), and (4) agree to sign the Informed consent and (5) are willing to attend follow up and / or electroacupuncture sessions.

Exclusion criteria

Exclusion criteria: Patients with symptoms and signs of axonal loss and evident median nerve denervation, including 1. constant numbness; 2. loss of sensibility, and 3. thenar muscular atrophy or weakness will be excluded. Patients with secondary CTS caused by inflammatory arthropathy, coexisting cervical radical radiculopathy, polyneuropathy, diabetes mellitus, pregnancy, malignancy, hypothyroidism, alcoholism, rheumatoid arthritis, space-occupying lesions (tumours, hypertrophic synovial tissue, fracture callus, and osteophytes), infections, and familial neuropathy will also be excluded. In particular, cervical radiculopathy will be actively ruled out by assessing the existence of related symptoms and signs, including neck pain, reduced reflexes, less well demarcated dermatomal involvement, and positive Spurling's test. Patients who received previous carpal tunnel release surgery, or have used warfarin, oral steroid, local steroid injection, night splint or acupuncture for CTS in the past 6 months, or other serious illnesses will be considered as ineligible.

Design outcomes

Primary

MeasureTime frame
Boston Carpal Tunnel Questionnaire Scoring at 1, 2, 5 and 17 weeks;

Secondary

MeasureTime frame
1. Disabilities of the Arm, Shoulder, and Hand (DASH) Questionnaire;2. A 0 to 10 point numerical rating scale to measure pain intensity.;3. Tip pinch strength (TPS);4. Semmes-Weinstein monofilament testing (SWMT);5. Dellon-modified Moberg pick-up test (DMMPUT);

Countries

China

Contacts

Public ContactVincent Chi Ho, Chung
vchung@cuhk.edu.hk+852 22528759

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 1, 2026