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Clinical Trials/NCT00353847
NCT00353847
Unknown
Phase 3

A Randomized, Single Blind, Controlled Clinical Trial to Evaluate the Pain Relief Efficacy, Functional Improvement and Safety of Acupuncture in Patients With Chronic Low Back Pain

Korea Institute of Oriental Medicine1 site in 1 country50 target enrollmentJuly 2006

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Chronic Low Back Pain
Sponsor
Korea Institute of Oriental Medicine
Enrollment
50
Locations
1
Primary Endpoint
Visual Analogue Scale, RDQ scale
Last Updated
19 years ago

Overview

Brief Summary

The purpose of this study is to determine whether acupuncture is effective and safe in the treatment of chronic LBP.

Detailed Description

The purpose of this study is as follows: 1. pain : VAS 2. Function : Roland Disability Scale 3. Side effect 4. Validity

Registry
clinicaltrials.gov
Start Date
July 2006
End Date
TBD
Last Updated
19 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Having chronic, non-specific, LBP of at least 3 months' duration over 20 years old.
  • Back pain must be the chief complaint
  • Having normal neurological test
  • Having signature voluntarily an IRB-approved consent form at enrollment

Exclusion Criteria

  • Potential spinal disease (e.g. a spinal tumor, infection or fracture etc)
  • Other diseases (e.g. bleeding disease, dementia,epilepsy, neurogenic disorder etc)
  • Planned or got lumbar surgery
  • The prior use of acupuncture within the past 6 months
  • Inflammatory arthritis
  • The current use of systematic corticosteroids, narcotics, anticoagulants, muscle relaxants
  • The involvement in legal problem related to LBP
  • Refusal to be randomized

Outcomes

Primary Outcomes

Visual Analogue Scale, RDQ scale

Secondary Outcomes

  • Patient Global Assessment

Study Sites (1)

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