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Analysis of factors affecting the postoperative effects of traditional open fusion surgery and minimally invasive fusion surgery or full-endoscopic spine surgery in the treatment of lumbar disc herniation and spinal stenosis

Analysis of factors affecting the postoperative effects of traditional open fusion surgery and minimally invasive fusion surgery or full-endoscopic spine surgery in the treatment of lumbar disc herniation and spinal stenosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200056099
Enrollment
Unknown
Registered
2022-02-01
Start date
2022-02-15
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

lumbar disc herniation, spinal stenosis

Interventions

Lumbar disc herniation treated by traditional open surgery group:none
Spinal stenosis treated by traditional open surgery group:none
Lumbar disc herniation treated by minimally invasive spine surgery group:none
Spinal stenosis treated by minimally invasive spine surgery group:none

Sponsors

Institute of Psychology, Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Men and women aged 20-80 years; 2.Patients diagnosed as lumbar disc herniation or spinal stenosis based on medical history, physical signs and imaging; 3.Patients that will undergo traditional open fusion surgery, minimally invasive fusion surgery or full-endoscopic spine surgery due to lumbar disc herniation or spinal stenosis; 4.Able to express and communicate in Chinese; 5.Able to read and write Chinese; 6.Willingness to comply with trial procedures and regulations; 7.Willing and able to sign informed consent; 8.Complete follow-up information.

Exclusion criteria

Exclusion criteria: 1.History of serious mental illness, including major depression, schizophrenia, etc; 2.Lumbar infection, ankylosing spondylitis, or spinal tumor; 3.Patients with serious primary diseases of the heart, brain, liver, kidney and hematopoietic system, as well as patients with acute diseases, infectious diseases or malignant tumors; 4.Patients with cognitive impairment or personality disorder; 5.The researcher believes that the patient should not be included in this research.

Design outcomes

Primary

MeasureTime frame
Anxiety;Depression;Sleep quality;Post-traumatic stress disorder;Social support rating;Visual Analogue Scale;Oswestry Disability Index;

Countries

China

Contacts

Public ContactHu Li

Institute of Psychology, Chinese Academy of Sciences

huli@psych.ac.cn+86 18310227286

Outcome results

None listed

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