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Randomized controlled clinical trial of acupotomy for herniated lumbar disc: pilot study

Not Applicable
Recruiting
Conditions
Diseases of the musculo-skeletal system and connective tissue
Registration Number
KCT0002188
Lead Sponsor
Korea Institute of Oriental Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

1. A confirmed diagnosis of lumbar herniated disc by CT(Computed Tomography) or MRI(magnetic resonance imaging) within 5 years
2. at least one of following symptoms
1) Low back pain 2) radiating pain in low extremity 3) paraesthesia in low extremity
3. Males and females aged 20-80 years
4. Those who have no problems with language, expression and concentration
5. Able and willing to comply with intervention and follow-up evaluation
6. Voluntary agreement via written informed consent after being provided with an explanation regarding the purpose and characteristics of this study

Exclusion Criteria

Participants having one or more of the following criteria will be excluded:
1. History of hypersensitivity by acupuncture treatment
2. Patients requiring surgery because of cauda equina syndrome, or neurological symptoms such as motor and/or sensory paralysis
3. History of plate internal fixation or spinal fusion operation
4. History of neuromyopathic scoliosis or neurological degenerative disease
5. Pregnant woman, lactating woman, or woman in childbearing years who plans on being pregnant
6. Those who have a history of neurotic or psychiatric major disability or who are mentally or cognitively unstable
7. Those who are terminally ill, and need a active therapy for the illness
8. History of alcoholism or drug abuse
9. Those who have a hemorrhagic disease, uncontrolled diabetes, or cardiovascular disease, and/or factors that can affect hemostasis such as anti-coagulant or anti-platelet drug
10. Those who are considered as inappropriate for the study by researcher

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual Analogue Scale
Secondary Outcome Measures
NameTimeMethod
Oswestry Disability Index(ODI);Modified-Modified Schober Test(MMST);Quality of life(EuroQol five dimensions questionnaire; EQ-5D)
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