low back pain
Conditions
Interventions
Lateral endoscopic foraminal expansion and discectomy group:Lateral endoscopic foraminal expansion and discectomy group
Lateral endoscopic foraminal expansion and discectomy + PRP group:Lateral endoscopic foraminal expansion and discectomy + PRP group
Posterior lumbar fenestration decompression and discectomy group:Posterior lumbar fenestration decompression and discectomy group
Posterior lumbar fenestration decompression and discectomy +PRP group:Posterior lumbar fenestration decompression and discectomy +PRP group
Sponsors
The First Affiliated Hospital of Air Force Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Lateral endoscopic intervertebral foraminal enlargement and intervertebral disc removal group: 1) Subjects are aged 18-55 years old (including 18 years old and 55 years old), gender is not limited; 2) Patients diagnosed with lumbar intervertebral disc herniation and corresponding nerve root compression; 3) Single or double segment with protruding segments between L2-L5 and those who have not participated in other clinical validators within 3 months; 4) Those who have not undergone any spine and joint related surgeries within 6 months; 5) There is no improvement in non-surgical treatment that has been carried out for more than 3 months in the past year, and the existing commercial implants cannot meet the surgical needs; 6) Understand the study, voluntarily sign and provide informed consent; 7) Willing to complete the follow-up of the trial and the data collection during the study. 2. Posterior lumbar lamination decompression and intervertebral disc removal group: 1) Subjects are 18-65 years old (including 18 years old and 65 years old), gender is not limited; 2) Patients diagnosed with lumbar intervertebral disc herniation or single-segment spinal stenosis, corresponding nerve root compression; 3) Single or double segment with protruding segments between L2-S1 and those who have not participated in other clinical validators within 3 months; 4)Those who have not undergone any spine and joint related surgeries within 6 months; 5)There is no improvement in non-surgical treatment that has been carried out for more than 3 months in the past year, and the existing commercial implants cannot meet the surgical needs; 6) Understand the study, voluntarily sign and provide informed consent; 7) Willing to complete the follow-up of the trial and the data collection during the study.
Exclusion criteria
Exclusion criteria: (1) History of spinal trauma, fracture, infection, or tumor (2) History of previous spinal surgery; (3) Combined ankylosing spondylitis and other immunodeficiencies affecting the spine; (4) Severe pelvic and lower limb bone and joint diseases; (5) Back muscle trauma, infection and connective tissue disease; (6) Developmental delay.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS,Visual Analogue Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Imaging tests; | — |
Countries
China
Contacts
Public ContactGao bo
The First Affiliated Hospital of Air Force Medical University
Outcome results
None listed