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A retrospective study on the efficacy of "intradiscal annular decompression" under spinal endoscopy for lumbar disc herniation and its impact on the same-segment reoperation rate

A retrospective study on the efficacy of "intradiscal annular decompression" under spinal endoscopy for lumbar disc herniation and its impact on the same-segment reoperation rate

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121737
Enrollment
Unknown
Registered
2026-04-02
Start date
2026-04-02
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Low back pain and radiating pain in the lower limbs caused by lumbar disc herniation

Interventions

Conventional Discectomy:None
Intradiscal Circumferential Decompression:None

Sponsors

Army Medical Center of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-70, with no gender restrictions; 2.Unilateral lumbar disc herniation at a single level (L3/4, L4/5, L5/S1); 3.MRI examination reveals lumbar disc herniation with nerve root compression; 4.The patient exhibits clear symptoms of nerve root pain, which are consistent with the radiographic findings; 5.Conservative treatment for at least 6 weeks has been ineffective; 6.The clinical data are complete, with a follow-up period of >= 24 months;

Exclusion criteria

Exclusion criteria: 1.Multi-level lumbar disc herniation; 2.Disc herniation with free disc fragments at the distal end(extending beyond the upper and lower edges of the intervertebral space by 5mm); 3.Associated disc calcification; 4.Moderate or severe spinal stenosis; 5.Previous history of lumbar surgery; 6.Presence of lumbar instability or spondylolisthesis (dynamic X-ray vertebral slippage >3mm or intervertebral angle change >15°) or lumbar spondylolisthesis (>=Grade I); 7.Concurrent lumbar infection or tumor; 8.Patients with severe internal diseases that are intolerable to surgery; 9.Incomplete clinical data or loss to follow-up;

Design outcomes

Primary

MeasureTime frame
postoperative recurrence;

Countries

China

Contacts

Public ContactLiuPeng

Army Medical Center of PLA

liupengd@163.com+86 23 68729291

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026