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Clinical Trials/NCT03879447
NCT03879447
Active, not recruiting
Not Applicable

Observational Study on the Effectiveness and Safety of Integrative Korean Medicine Treatment for Patients With Low Back Pain or Sciatica Due to Lumbar Stenosis or Spondylolisthesis

Jaseng Medical Foundation1 site in 1 country110 target enrollmentJune 24, 2019

Overview

Phase
Not Applicable
Intervention
Herbal medicine
Conditions
Lumbar Spinal Stenosis
Sponsor
Jaseng Medical Foundation
Enrollment
110
Locations
1
Primary Endpoint
Change in Numeric rating scale (NRS) of higher score at baseline out of low back pain or radiating leg pain
Status
Active, not recruiting
Last Updated
4 months ago

Overview

Brief Summary

A prospective observational study investigating the effectiveness and safety of integrative Korean medicine treatment in lumbar stenosis or spondylolisthesis patients with low back pain or sciatica at 3 locations of Jaseng Hospital of Korean Medicine as assessed through of pain, functional disability, walking ability, and quality of life patient-reported outcomes

Detailed Description

This is a prospective observational study to the aim of investigating the effectiveness and safety of integrative Korean medicine treatment (generally consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, and cupping) in lumbar stenosis or spondylolisthesis patients with low back pain or sciatica diagnosed by lumbar X-ray and/or MRI and clinical symptoms including neurogenic claudication at 3 locations of Jaseng Hospital of Korean Medicine (Bucheon, Daejeon, Busan (Haeundae)) as assessed through of pain, functional disability, walking ability, and quality of life patient-reported outcomes with a 5-year follow-up period

Registry
clinicaltrials.gov
Start Date
June 24, 2019
End Date
December 1, 2027
Last Updated
4 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

In-Hyuk Ha, KMD

Director

Jaseng Medical Foundation

Eligibility Criteria

Inclusion Criteria

  • Patients with radiating leg pain or low back pain (LBP) intensity of NRS ≥5
  • Patients diagnosed with lumbar stenosis based on dural sac cross-sectional area (DSCA) of \<100 mm2 or morphological grading ≥B as assessed on MRI; or patients diagnosed with lumbar spondylolisthesis based on Meyerding Grade Ⅱ or higher as assessed on X-ray
  • Clear neurogenic claudication symptoms (symptoms aggravated with walking, and alleviated upon resting in lumbar flexion position), if lumbar stenosis patient
  • Patients with plans of receiving Korean medicine treatment for lumbar spinal stenosis for ≥4 months
  • Patients who have agreed to study participation

Exclusion Criteria

  • Patients with vascular claudication
  • Patients with other systemic diseases that may interfere with treatment effect or outcome interpretation
  • Patients with soft tissue pathologies or pathologies of non-spinal origin that may cause LBP or radiating leg pain (e.g. spinal tumor, rheumatoid arthritis)
  • Patients for whom acupuncture treatment may be inappropriate or unsafe (e.g. hemorrhagic diseases, blood clotting disorders, history of anti-coagulation medicine intake, serious diabetes with risk of infection, severe cardiovascular diseases, or other conditions deemed unsuitable for acupuncture treatment)
  • Patients with medical history of spinal surgery within the past 3 months
  • Patients who were treated with invasive interventions such as Korean medicine treatment, injections, physical therapy, or with medicine that may potentially influence pain such as NSAIDs (nonsteroidal antiinflammatory drugs) within the past week
  • Pregnant patients or patients planning pregnancy
  • Patients with serious psychological disorders
  • Previous participation in other clinical studies within 1 month of current study enrollment, or plans to participate in other clinical studies during participation (including follow-up period) of the current study after study enrollment
  • Patients unable to fill out study participation consent form

Arms & Interventions

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Herbal medicine

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Chuna manual medicine

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Bee venom pharmacopuncture

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Pharmacopuncture

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Acupuncture

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Electroacupuncture

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Cupping

Lumbar stenosis group

Lumbar stenosis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Other intervention(s)

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Herbal medicine

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Chuna manual medicine

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Bee venom pharmacopuncture

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Pharmacopuncture

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Acupuncture

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Electroacupuncture

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Cupping

Lumbar spondylolisthesis group

Lumbar spondylolisthesis patients will be administered integrative Korean medicine treatment consisting of herbal medicine, Chuna manual medicine, bee venom pharmacopuncture and pharmacopuncture, acupuncture, electroacupuncture, cupping, and other interventions, as needed.

Intervention: Other intervention(s)

Outcomes

Primary Outcomes

Change in Numeric rating scale (NRS) of higher score at baseline out of low back pain or radiating leg pain

Time Frame: Change from baseline to 4 months

Change from higher score at baseline out of low back pain or radiating leg pain intensity to same score at 4 months. Total score range: -10 (worse outcome) to 10 (better outcome)

Secondary Outcomes

  • Numeric rating scale (NRS) of radiating leg pain(Baseline, observation at least once a week for the duration of active treatment up to a maximum of 24 weeks (2, 4, 6, 8, 12, 16, 20, 24 weeks), 1, 3, 5 years)
  • Visual analogue scale (VAS) of radiating leg pain(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • Maximum walking distance (average of the past 3 days)(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • Oswestry Disability Index (ODI)(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • EQ-VAS(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • SF-36([Time Frame: Baseline, 4, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years])
  • Numeric rating scale (NRS) of low back pain(Baseline, observation at least once a week for the duration of active treatment up to a maximum of 24 weeks (2, 4, 6, 8, 12, 16, 20, 24 weeks), 1, 3, 5 years)
  • Visual analogue scale (VAS) of low back pain(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • Pain-free walking distance (average of the past 3 days)(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • Zurich Claudication Questionnaire(Baseline, 4, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • EuroQol 5-dimensions 5-levels (EQ-5D-5L)(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • Adverse reaction(Baseline, every visit for the duration of active treatment up to a maximum of 24 weeks (2, 4, 6, 8, 12, 16, 20, 24 weeks), 1, 3, 5 years)
  • Patient Global Impression of Change (PGIC)(8, 16, 20, 24 weeks, 1, 3, 5 years)
  • Physical examination(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)
  • Use of other intervention(s)(Baseline, 2, 4, 6, 8, 12, 16, 20, 24 weeks, 1, 3, 5 years)

Study Sites (1)

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