Carpal Tunnel Syndrome Treated With 830nm Diode Laser (CTS)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2007 by Chung Shan Medical University.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
National Taiwan University
Information provided by:
Chung Shan Medical University
ClinicalTrials.gov Identifier:
NCT00514462
First received: August 8, 2007
Last updated: August 9, 2007
Last verified: August 2007
  Purpose

The purpose of this study is to determine that 830nm diode laser directly above the transverse carpal ligament (between the pisiform and navicular bone) on subjects' wrists, and test this therapeutic effect.


Condition Intervention Phase
Carpal Tunnel Syndrome
Device: diode laser
Phase 1
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
Official Title: Instiutional Review Board of Chung Shan Medical University Hospital

Resource links provided by NLM:


Further study details as provided by Chung Shan Medical University:

Primary Outcome Measures:
  • treatment effect [ Time Frame: two weeks ]

Secondary Outcome Measures:
  • EMG, Jamar dynamometer, Carpal tunnel function disability form [ Time Frame: two weeks ]

Estimated Enrollment: 30
Study Start Date: July 2007
Estimated Study Completion Date: August 2007
Arms Assigned Interventions
Experimental: A
low level laser instrument (Painless Light PL-830, Advanced Chips & Products Crop., USA)
Device: diode laser
wavelength at 830nm, 9.7J/cm2 for 10 min
Other Name: Low-level laser

Detailed Description:

The low level laser instrument (Painless Light PL-830, Advanced Chips & Products Crop., USA) emitted two light beams with a distance of 2.5cm between them by two laser diodes.

  Eligibility

Ages Eligible for Study:   18 Years to 70 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • no operation of the wrist
  • first onset of CTS more than 1 year ago with repeated episodes
  • never having laser treatment before.

Exclusion Criteria:

  • patients with any rheumatoid arthritis
  • history of metabolic disease or paralyzed limbs caused by stroke
  • taking any anti-inflammatory drug
  • with other treatments, such as acupuncture, physical therapy and wearing orthosis
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00514462

Contacts
Contact: Yu-Chun Yeh, Ph.D 886922002769 mandy-steven@yahoo.com.tw

Locations
China, Taiwan
Chung Shan Medical University Hospital Recruiting
Chinese Taipei, Taiwan, China, 360
Contact: Joe-Air Jiang, Ph.D    886-2-33665341    jajiang@ntu.edu.tw   
Sponsors and Collaborators
Chung Shan Medical University
National Taiwan University
Investigators
Study Director: Chin-Ping Han, MD/PhD Chung Shan Medical University Hospital
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00514462     History of Changes
Other Study ID Numbers: CS07040
Study First Received: August 8, 2007
Last Updated: August 9, 2007
Health Authority: Taiwan: Department of Health

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 July 23, 2014