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Comparative analysis of the efficacy of day surgery and non day surgery in the treatment of lumbar disc herniation with spinal endoscopy

Comparative analysis of the efficacy of day surgery and non day surgery in the treatment of lumbar disc herniation with spinal endoscopy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040887
Enrollment
Unknown
Registered
2020-12-13
Start date
2020-12-01
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

lumbar degenerative disease

Interventions

day-surgery:Discharge within 24 hours
non day-surgery:Discharge after 24 hours

Sponsors

The Second Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) The patients were diagnosed as single level lumbar disc herniation; (2) Conservative treatment was ineffective; (3) After comprehensive evaluation, it can tolerate spinal endoscopic surgery; (4) Be able to comply with the requirements of the research protocol until the completion of the study; (5) Patients who agreed to enter the clinical study and voluntarily signed the written informed consent.

Exclusion criteria

Exclusion criteria: (1) There were clear contraindications such as severe coagulation system disease and severe liver and kidney insufficiency; (2) Patients with infection or tuberculosis; (3) Patients who could not tolerate anesthesia and spinal endoscopic surgery; (4) Pregnant or lactating women; (5) Those who have participated in other clinical trials in recent 3 months and have not reached the end point; (6) Patients with multi segmental disc herniation; (7) Patients with lumbar spondylolisthesis; (8) Subjects who were unable to communicate or did not follow the instructions; (9) The researcher thinks that it is not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale;Oswestry Disability Index;Modified macnab evaluation of curative effect;Incidence of postoperative complications;hospital costs;

Secondary

MeasureTime frame
Length of stay;

Countries

China

Contacts

Public ContactXigao Cheng

The Second Affiliated Hospital of Nanchang University

228206846@qq.com+86 1387065428

Outcome results

None listed

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