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A Multicenter Clinical Efficacy Evaluation Study on Integrated Traditional Chinese and Western Medicine Treatment for Lumbar Disc Herniation Based on the Theory of "Gu cuo feng jin chu cao"

A Multicenter Clinical Efficacy Evaluation Study on Integrated Traditional Chinese and Western Medicine Treatment for Lumbar Disc Herniation Based on the Theory of "Gu cuo feng jin chu cao"

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001254
Enrollment
Unknown
Registered
2025-06-23
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Lumbar Disc Herniation

Interventions

Treatment group:The patients are treated with Zheng's reduction manipulation for "Gu cuo feng jin chu cao" of the lumbar spine once a day. The treatment is carried out one day and two days before the
Control group:Percutaneous Endoscopic Lumbar Discectomy (PELD) surgery is adopted.

Sponsors

Sichuan Orthopedic Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Aged between 18 and 65 years old; (2) Meeting the above diagnostic criteria with symptoms and signs predominantly involving the unilateral lower limb; (3) All patients have single-segment lumbar disc herniation; (4) Patients who fail to respond to systematic conservative treatment for 4 to 6 weeks or those with severe pain due to lumbar disc herniation who after clear diagnosis and exclusion of contraindications undergo surgical treatment directly without conservative treatment; (5) Meeting the surgical indications for spinal endoscopic treatment of lumbar disc herniation; (6) Patients who have signed the informed consent form and are willing to cooperate with outpatient follow-ups and telephone reviews.

Exclusion criteria

Exclusion criteria: (1) Imaging examinations suggest concomitant lumbar deformity lumbar instability at the lesion segment severe calcification or lumbar spinal stenosis; (2) History of spinal surgery combined with spinal infection severe osteoporosis or tumor; (3) Concomitant severe cardiovascular and cerebrovascular diseases; (4) Concomitant cauda equina nerve injury and progressive peripheral nerve injury; (5) Suffering from mental disorders or poor compliance unable to cooperate with evaluators; (6) Currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Oswestry Disability Index (ODI);

Secondary

MeasureTime frame
Macnab;SF-12;VAS;

Countries

china

Contacts

Public ContactWu ji

Sichuan Orthopedic Hospital

239993809@qq.com13438281260

Outcome results

None listed

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