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A randomized controlled clinical study on the treatment of lumbar disc herniation with neurolysis under anesthesia

A randomized controlled clinical study on the treatment of lumbar disc herniation with neurolysis under anesthesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041958
Enrollment
Unknown
Registered
2021-01-10
Start date
2021-02-01
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

Nerve root adhesion in lumbar disc herniation

Interventions

Experimental group:Shi’s manual therapy under under continuous epidural anesthesia
Control group:Sham manipulation under under continuous epidural anesthesia

Sponsors

Shuguang Hospital Affiliated to Shanghai University of TCM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who meet the diagnostic criteria of nerve root adhesion in lumbar disc herniation; 2. Patients with ODI >= 10; 3. The age is between 20 and 70 years old; 4. Patients who voluntarily join the study and sign "informed consent" after informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with lumbar disc herniation without nerve root adhesion; 2. Patients with lumbar disc herniation with cauda equina and lower extremity motor nerve injury; 3. Patients who have received spinal surgery; 4. For patients with a history of severe spinal trauma, spinal bone lesions such as spinal fracture, dislocation, spinal tuberculosis, scoliosis, spinal instability, spinal tumor, severe lumbar degenerative changes, and other spinal bone lesions were detected by imaging examination; 5. Patients with local soft tissue rupture or infectious inflammatory lesions; 6. Patients with cardiovascular, cerebrovascular, hematopoiesis, digestive system, and other serious diseases or mental disorders; 7. Pregnant or lactating women; 8. Patients who are considered unsuitable or unwilling to join the study.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale, VAS;Oswestry Disability Index, ODI;Angle of straight leg raising test;

Countries

China

Contacts

Public ContactZhan Hongsheng

Shuguang Hospital Affiliated to Shanghai University of TCM

13918449223@139.com+86 13918449223

Outcome results

None listed

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