Completed

Phase 2
Age: 18Years - 70Years
All Genders
ID00000394

A Controlled Trial of Acupuncture for Carpal Tunnel Syndrome

Led by George Washington University · Updated on 2013-05-15

144

Participants Needed

N/A

Research Sites

N/A

Total Duration

On this page

Sponsors

G

George Washington University

Lead Sponsor

N

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study will look at the effectiveness of acupuncture for treating carpal tunnel syndrome (CTS). People who participate in this study will have CTS that has been diagnosed by physical examination and neurological testing. We will randomly assign study participants to receive one of the three types of acupuncture either once, twice, or three times weekly for a total of 6 weeks. Acupuncturists will treat one group of patients with true acupuncture. They will give the other two groups of patients one of two alternative acupuncture treatments that do not use the true acupuncture points. The patients and evaluators will not know the type of acupuncture (True, Alternative 1, or Alternative 2) that is being used. The acupuncturists will not communicate with the patients and will not be involved in patient evaluation.

CONDITIONS

Official Title

Acupuncture for Carpal Tunnel Syndrome

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Hand or wrist pain combined with parathesias or numbness in any or all fingers, predominating in a median nerve distribution, and especially occurring at night
  • Symptoms unresponsive or poorly responsive to standard conservative therapy (wrist splints, analgesics, nonsteroidal anti-inflammatory drugs)
  • Electrodiagnostic evidence of distal median neuropathy compatible with carpal tunnel syndrome (to be confirmed at study site)
  • Symptoms present for at least 3 months
  • No prior treatment with acupuncture for carpal tunnel syndrome
Not Eligible

You will not qualify if you...

  • Evidence of pronounced abductor pollicis weakness or significant thenar wasting (probable candidate for carpal tunnel surgery)
  • Prior carpal tunnel surgery on affected side
  • Use of narcotic analgesia
  • History of wrist or hand fracture on the symptomatic limb
  • Current pregnancy or less than 3 months postpartum
  • Corticosteroid injection into the carpal tunnel within 3 months
  • History of generalized peripheral neuropathy or clinical or electrodiagnostic evidence of generalized polyneuropathy or mononeuropathy multiplex
  • History of other neurologic disorders which may cause confusion with the diagnosis of carpal tunnel syndrome, including but not limited to stroke, cervical radiculopathy, myelopathy, subdural hematoma, brain tumor
  • Inflammatory articular disease or tendinitis of the hand or wrist by history or physical examination
  • Insulin-dependent diabetes mellitus
  • Clinical hypothyroidism
  • Chronic renal failure or renal dialysis or forearm fistulae
  • Other disorder known to predispose to carpal tunnel syndrome including acromegaly, multiple myeloma, amyloidosis

Trial Site Locations

Site Locations not provided

Location information for this trial is currently unavailable.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

0

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