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A Multicenter Clinical Study on Integrated Rehabilitation Therapy for Lumbar Disc Herniation Based on the Empirical Decomposition of the (Jin-Gu-Tiao-Heng) Approach

A Multicenter Clinical Study on Integrated Rehabilitation Therapy for Lumbar Disc Herniation Based on the Empirical Decomposition of the (Jin-Gu-Tiao-Heng) Approach

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000477
Enrollment
Unknown
Registered
2026-03-05
Start date
2026-03-18
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lumbar Disc Herniation

Interventions

Normal control group:Non-interference
The basic drug therapy control group.:Dehydration treatment, analgesia, promoting blood circulation and anti-inflammatory effects, etc., as symptomatic treatment.
Experimental Group A:Tuina + Acupuncture
Trial Group B:Formulation Group
Experimental Group C:Tuina + Acupuncture + Formulation group

Sponsors

Kunshan Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: According to the "Criteria for Diagnosis and Therapeutic Efficacy of Chinese Medicine Diseases" issued by the National Administration of Traditional Chinese Medicine, the following standards are referenced: 1. There is a history of lumbar trauma, chronic strain, or exposure to cold and dampness. Most patients have a history of chronic low back pain before the onset of the disease. 2. Lumbar pain may be accompanied by numbness and radiation in the buttocks and lower extremities. The pain worsens with increased abdominal pressure (e.g., coughing or sneezing). 3. Spinal scoliosis is present, with the physiological curvature of the lumbar spine disappearing or becoming kyphotic. Tenderness is present at the affected vertebral segments, which may radiate to the lower extremities. Lumbar mobility is significantly restricted. 4. The affected nerve distribution areas of the lower extremities exhibit sensory hypersensitivity or hypoesthesia. In long-standing cases, muscle atrophy may occur. The straight leg raise test or its reinforcement test is positive, knee and Achilles tendon reflexes are diminished or absent, and dorsiflexion or plantar flexion strength of the great toe is weakened. 5. X-ray examination may show: spinal scoliosis, disappearance of the physiological anterior convexity of the lumbar spine, possible narrowing of the intervertebral disc space, and osteophyte proliferation at adjacent margins. CT examination may show: the location and degree of intervertebral disc protrusion, and assessment of lumbar spinal canal stenosis. MRI examination may show: intervertebral disc degeneration, high-signal zones posterior to the annulus fibrosus, nucleus pulposus protrusion, compression of the dural sac and nerve roots, and differentiation from intraspinal tumors. Imaging examinations aid in confirming the diagnosis and selecting appropriate treatment methods. 6. The patient has signed an informed consent form, is willing to undergo the rehabilitation treatment plan, and the clinical diagnostic and treatment process conforms to medical ethical standards.

Exclusion criteria

Exclusion criteria: 1) Those who do not meet the above inclusion criteria. 2) Patients with lumbar spondylolisthesis of grade II or higher,. Patients with lumbar spondylolisthesis of grade II or higher, isthmic spondylolisthesis, or significant lumbar instability. 3) Patients with significant lumbar spinal stenosis, hypertrophy, or calcification of the ligamentum flavum. 4) Patients with abnormal bowel or bladder function, saddle anesthesia, or other symptoms of cauda equina syndrome. 5) Patients with a history of tumors, tuberculosis, blood disorders, infections, or allergies to related medications. 6) Patients with deficits in lower extremity motor function,, hyperactive tendon reflexes, ankle clonus, or other signs of upper motor neuron or spinal cord lesions. 7) Patients with gait abnormalities such as weakness, festination, swaying, or ataxia, suggesting possible central, spinal cord, or skeletal muscle abnormalities. 8) Patients with severe cardiovascular, cerebrovascular, liver, or kidney diseases; poorly controlled diabetes; or severe mental illness that poses a serious threat to life. 9) Patients with weak physical condition or severe osteoporosis. 10) Pregnant women, breastfeeding women, and women during menstruation.

Design outcomes

Primary

MeasureTime frame
Medical Outcomes Survey Short Form-36;Oswestry Disability Index;

Secondary

MeasureTime frame
Hamilton Rating Scale for Depression,HRSD-17);Hamilton Rating Scale for Anxiety;

Countries

China

Contacts

Public ContactDAI DECHUN

Kunshan Hospital of Chinese Medicine

dechundai@163.com13862605581

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026