To Investigate the Therapeutic Effect of Aculife Magnetic Therapist on Carpal Tunnel Syndrome
Recruitment status was Recruiting
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Purpose
Carpal tunnel syndrome (CTS) is the most common compressive focal mononeuropathy seen in clinical practice. Patients commonly experience a constellation of symptom complex brought on by compression of the median nerve as it traverse through the carpal tunnel. When compression of the nerve occurs, ischemia and mechanical disruption of nerve function may result. Pathological analysis shows a constellation of nerve injuries. Until now, no satisfactory conservative treatment method. Local steroid injections or oral steroids may result in initial relief, but relapses are frequent and have much side effects, which preclude their routine use for CTS. Full time wrist splints are claimed effective, but compromise hand function and daily activities. There are reasonable studies showing relief of pain with acupuncture on diverse pain conditions. However the therapeutic efficacy of acupuncture in CTS was less convincing in the past. Until recent decade, some case reports and few prospective studies reported the therapeutic effect of acupuncture in CTS. Other study also reported that low-level laser and microamperes transcutaneous electrical nerve stimulation (TENS) are effective in improvement of clinical outcome of patients with CTS. Another report suggested that TENS should be considered for the treatment of painful diabetic peripheral neuropathy. Therefore, the investigators perform this study to evaluate the effect of Aculife Magnetic Wave Therapist (a battery operated device with a probe electrode which contains magnetic elements that transform the oscillating current into an electromagnetic wave to stimulate the acupuncture points, simulate the effect of electroacupuncture ) on CTS and compared with that of Transcutaneous Electrical Nerve Stimulation(TENS). After at least 4 weeks treatment ( at least 16 treatment sessions) the therapeutic effects will be evaluated by comparison of symptom severity score, electrophysiological study, sonographic morphology study or magnetic resonance imaging study, before and after treatment, and between the different groups.
| Condition | Intervention |
|---|---|
|
Carpal Tunnel Syndrome |
Device: Aculife Magnetic Wave Therapist Device: TENS |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: Single Blind (Investigator) Primary Purpose: Treatment |
| Official Title: | To Investigate the Therapeutic Effect of Aculife Magnetic Therapist on Carpal Tunnel Syndrome |
- nerve conduction study [ Time Frame: after at least four weeks treatment (at least 16 treatment sesstions) ] [ Designated as safety issue: No ]
- questionnaire [ Time Frame: after at least four weeks treatment ( at least 16 treatment sesstions) ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 30 |
| Study Start Date: | December 2010 |
| Estimated Primary Completion Date: | February 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Aculife Magnetic Wave Therapist
patients with carpal tunnel syndrome treated with Aculife
|
Device: Aculife Magnetic Wave Therapist
two therapeutic points, each for 15 minutes
|
|
Active Comparator: TENS
patients with carpal tunnel syndrome treated by TENS
|
Device: TENS
tow therapeutic points, each for 15 minutes
|
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- electrodiagnostic study confirmed with carpal tunnel syndrome
- clinical symptom related to carpal tunnel syndrome
Exclusion Criteria:
- hypothyroidism, gout, systemic lupus erythematosus, rheumatoid arthritis, diabetes mellitus, chronic renal failure, acromegaly, polyneuropathy, brachial plexopathy, proximal median nerve entrapment, deficiency neuropathy (vitamine 2, B12, ect.), drug usage that may cause neuropathy, any surgery for peripheral nerve in the upper limb such as carpal tunnel surgical release, history of trauma in the upper limb such as wrist fracture, or having pregnancy.
Contacts and Locations| Contact: Sui Foon Lo | d4659@mail.cmuh.org.tw |
| Taiwan | |
| China Medical University | Recruiting |
| Taichung, Taiwan, 404 | |
| Contact: Sui Foon Lo d4659@mail.cmuh.org.tw | |
More Information
No publications provided
| Responsible Party: | China Medical University Hospital |
| ClinicalTrials.gov Identifier: | NCT01277003 History of Changes |
| Other Study ID Numbers: | 0994266G |
| Study First Received: | January 13, 2011 |
| Last Updated: | January 18, 2011 |
| Health Authority: | Taiwan: Institutional Review Board |
Additional relevant MeSH terms:
|
Carpal Tunnel Syndrome Median Neuropathy Mononeuropathies Peripheral Nervous System Diseases Neuromuscular Diseases |
Nervous System Diseases Nerve Compression Syndromes Cumulative Trauma Disorders Sprains and Strains Wounds and Injuries |
ClinicalTrials.gov processed this record on May 23, 2013