Observational Study on Effectiveness and Safety of Integrative Korean Medicine Treatment for Inpatients With Sciatica Due to Lumbar Intervertebral Disc Herniation

Jaseng Medical Foundation1,000 enrolled

Overview

Observational study on the effectiveness and safety of integrative Korean medicine treatment for inpatients with sciatica due to lumbar intervertebral disc herniation

Establishment of a Korean medicine inpatient treatment registry of inpatients with sciatica due to lumbar intervertebral disc herniation with or without spinal stenosis, in conjunction with an observational study to the aim of evaluating the effectiveness and safety of Korean medicine treatment for inpatients

Study Type

OBSERVATIONAL

Enrollment

1,000

Conditions

Sciatica Due to Intervertebral Disc Disorder Intervertebral Disc Displacement Sciatica Sciatic Radiculopathy

Interventions

Herbal medicineDRUG

Herbal medicine will be mainly administered in water-based decoction (120ml) and dried powder (2g) form (the ingredients are mainly, but not restricted to: Ostericum koreanum, Eucommia ulmoides, Acanthopanax sessiliflorus, Achyranthes japonica, Psoralea corylifolia, Saposhnikovia divaricata, Cibotium barometz, Lycium chinense, Boschniakia rossica, Cuscuta chinensis, Glycine max, Atractylodes japonica).

Chuna manual therapyPROCEDURE

Chuna is a Korean spinal manipulation that incorporates spinal manipulation techniques for joint mobilization involving highvelocity, low amplitude thrusts to joints slightly beyond the passive range of motion and gentle force to joints within the passive range of movement. Chuna manipulation will be administered at the physician's discretion.

Bee venom pharmacopuncture

Eligibility

Sex: ALLMin age: 19 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Lumbar intervertebral disc herniation as confirmed by a doctor of medicine or a doctor of Korean medicine through an MRI taken within 3 years 2. Patients with radiculopathy (ipsilateral or bilateral radiculopathy) 3. Patients whose pain intensity of back pain or radiating leg pain is NRS≥5 4. Patients aged 19 to 70 5. Patients who have agreed to participate in the clinical study and given written informed consent 6. Patients admitted to a Korean medicine hospital for treatment Exclusion Criteria: 1. Patients who have been diagnosed with a serious disease that may cause low back pain or neck pain (e.g. spinal metastasis of tumor, acute fracture, spinal dislocation) 2. Patients admitted due to pain caused by traffic accidents 3. Patients with progressive neurological deficit or severe neurological symptoms such as spinal cord injury 4. Patients with severe mental illness 5. Patients with difficulty or refusal to give sign written informed consent 6. Patients for whom the researchers judge participation in the clinical study to be difficult 7. Diagnosis of lumbar spondylolisthesis of Meyerding Ⅱ or higher by a doctor of medicine or doctor of Korean medicine through X-ray or MRI

Locations (4)

Bucheon Jaseng Hospital of Korean Medicine

Bucheon-si, Gyeonggi Province, South Korea

Haeundae Jaseng Hospital of Korean Medicine

Busan, South Korea

Daejeon Jaseng Hospital of Korean Medicine

Daejeon, South Korea

Jaseng Hospital of Korean Medicine

Seoul, South Korea

Outcomes

Primary Outcomes

NRS change from Baseline NRS at discharge

Numeric rating scale (NRS) of low back pain, and radiating leg pain In pain measurement using NRS, patients are asked to rate their pain by selecting a number from 0 to 10 that best represents their pain severity between the anchors of 0 which indicates 'no pain', and 10 which indicates 'worst pain possible'.

Time frame: Baseline (admission), discharge (up to 14 weeks after baseline)

ODI change from Baseline ODI at discharge

Oswestry Disability Index(ODI) The ODI evaluates functional impairment and is a 10-item questionnaire developed to assess the level of disability due to back pain. Each item is graded into 6 levels, each representing a score of 0-5. Higher scores indicate greater limitation relating to back pain.

Time frame: Baseline (admission), discharge (up to 14 weeks after baseline)

PGIC

Patient global impression of change (PGIC) PGIC grades the level of subjective improvement into 7 levels (1, very much improved; 2, much improved; 3, slightly improved; 4, no change; 5, slightly worse; 6, much worse; and 7, very much worse).

Time frame: 6 months after baseline

Secondary Outcomes

EQ-5D change from Baseline EQ-5D at each time point

EuroQol-5 Dimension(EQ-5D) EQ-5D is a tool developed for health-related quality of life (HRQoL) assessment, and is widely used in the health care sector. Scores range from -1, 'health worse than death' to 1, 'perfect health'. EQ-5D-5L has 5 dimensions covering current health status and functionality: mobility (M), self care (SC), usual activities (UA), pain/discomfort (PD), and anxiety/depression (AD), to be rated out of 5 grades (1, no problem; 2, slight problem; 3, some/moderate problem; 4, severe problem; 5, extreme problem).

Time frame: Baseline (admission), 2 weeks after baseline, discharge (up to 14 weeks after baseline), 6 months after baseline

Data from ClinicalTrials.gov

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Bee venom pharmacopuncture will be administered only after confirming a negative response to hypersensitivity skin test. Diluted bee venom (saline:bee venom ratio, 10,000:1) filtered for allergens will be injected at 4-5 acupoints proximal to the dysfunctional site at the physician's discretion. Each acupuncture point will be injected to a total of 0.5-1 cc using disposable injection needles (CPL, 1 cc, 26gauze(G) x 1.5 syringe, Shinchang medical co., Korea).

PharmacopuncturePROCEDURE

Pharmacopuncture consisting of select herbal ingredients will be administered at Ah-shi points and local acupuncture points using disposable injection needles (CPL, 1 cc, 26gauze(G) x 1.5 syringe, Shinchang medical co., Korea).

AcupuncturePROCEDURE

Acupuncture treatment will be administered using mainly proximal acupuncture points and Ah-shi points.

ElectroacupuncturePROCEDURE

Electroacupuncture treatment will be administered using mainly proximal acupuncture points and Ah-shi points.

CuppingPROCEDURE

Cupping treatment will be administered at 1-2 points using mainly proximal acupuncture points and Ah-shi points.

Other intervention(s)OTHER

Patients will be allowed any other additional intervention(s) as deemed necessary by the attending physician regardless of type or dose, and patterns of use will be investigated and recorded as an pragmatic clinical study.

Lumbar ROM from Baseline Lumbar ROM at each time point

Lumbar Range of Motion(ROM) (Flexion/Extension/Lateral flexion/Rotation) Pain upon movement in lumbar range of motion (ROM) will be assessed.

Time frame: Baseline (admission), 2 weeks after baseline, discharge (up to 14 weeks after baseline)

SLR from Baseline SLR at each time point

Straight Leg Raise test(SLR) The straight leg raise(SLR)is a test done during a physical examination to determine whether a patient with low back pain has an underlying herniated disc, often located at L5 (fifth lumbar spinal nerve). If the patient experiences sciatic pain when the straight leg is at an angle of between 30 and 70 degrees, then the test is positive and a herniated disk is a possible cause of the pain.\[3\] A negative test suggests a likely different cause for back pain.

Time frame: Baseline (admission), 2 weeks after baseline, discharge (up to 14 weeks after baseline)

Adverse events(AE) Physicians will monitor and record any unexpected or unintended patient reaction to integrative korean medicine at each visit. Adverse events (AEs) associated with integrative korean medicine will include, but not be limited to, AEs anticipated from previous reports of korean medicine, and will stay open to all possibilities taking into consideration other potential, unknown AEs.

Time frame: up to 14 weeks after baseline

NRS change from Baseline NRS at each timepoint

Time frame: Baseline (admission), 2 weeks after baseline, 6 months after baseline

ODI change from Baseline ODI at each timepoint

Time frame: Baseline (admission), 2 weeks after baseline, 6 months after baseline