Herniated lumbar disc
Conditions
Interventions
control group:Minimally invasive spinal disc removal surgery
experimental group:Minimally invasive spinal disc nucleotomy and annulus fibrosus suture
Sponsors
Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: (1) Age 18–80 years (including 18 and 80 years), no gender restrictions; (2) Meets Western medical diagnostic criteria for LDH; (3) Ineligible for surgical treatment after 3 months of conservative treatment; (4) Accurate and complete clinical data; (5) Anesthesia classification: Grade I–II; (6) CT scan shows no significant calcification or ossification, with the affected segment exhibiting a soft protrusion; after discectomy, the residual defect of the annulus fibrosus is <10 mm; (7) First-time surgical treatment, single-segment involvement; (8) Voluntarily participates in this trial and signs an informed consent form.
Exclusion criteria
Exclusion criteria: (1) Patients with malignant tumors, immune disorders, or hematological diseases; (2) Patients with a history of lumbar spine surgery; those with concomitant lumbar spine deformities, fractures, spondylolisthesis, endplate inflammation, or other lumbar spine conditions; (3) Patients with psychiatric disorders or cognitive impairments who cannot cooperate with the study; (4) Patients with severe impairment or failure of liver or kidney function; (5) Pregnant or breastfeeding women.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Recurrence rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual analogue scale;Oswestry dysfunction index;Spinal cord nerve function; | — |
Countries
China
Contacts
Public ContactRigao Chen
Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Outcome results
None listed