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Comparison of clinical efficacy of percutaneous transforaminal endoscopic discectomy in general anesthesia and local anesthesia

Comparison of clinical efficacy of percutaneous transforaminal endoscopic discectomy in general anesthesia and local anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000033240
Enrollment
Unknown
Registered
2020-05-25
Start date
2020-06-01
Completion date
Unknown
Last updated
2020-05-25

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

Conditions

lumbar disc herniation

Interventions

general anesthesia group:general anesthesia

Sponsors

Department of Spinal Orthopaedics, The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged from 18 to 65 years; 2.There is lumbar disc herniation in a single segment with corresponding manifestations of nerve damage, ranging from Radiation pain, sensory abnormality, motor dysfunction and reflex abnormality; 3.With conservative treatment ineffective for more than 3 months; 4.Clinical symptoms and signs were consistent with imaging findings; 5.The severity of the disease is up to the standard of surgical treatment; 6.No history of lumbar surgery; 7.Able to tolerate general anesthesia operation after anesthesia assessment made by anesthesiologist.

Exclusion criteria

Exclusion criteria: 1.Lumbar stenosis with slipping or instability requires surgical treatment; 2.Degenerative scoliosis requires surgical treatment; 3.Lumbar stenosis caused by other lumar diseases such as Ankylosing spondylitis and spinal tumor; 4.Metabolic diseases such as severe diabetes or severe osteoporosis; 5.Intermittent claudication caused by atherosclerosis; 6.Lower extremity joint dysfunction caused by Severe osteoarthritis or rheumatoid arthritis; 7.A neurological or psychiatric disorder, such as dementia or stroke, in which informed consent cannot be given; 8.After total hip or knee replacement.

Design outcomes

Primary

MeasureTime frame
Oswestry Disability Index;

Secondary

MeasureTime frame
SF-36 Health Survey Questionnaire;Visual analogue scale of low back pain;Visual analogue scale of lower extremity pain;Modified macnab efficacy evaluation criteria;duration of operation;blood loss;Related complications;Related complications;Reoperation rate;total hospitalization expenses;time in hospital altogether;

Countries

China

Contacts

Public ContactJiang Xiaobing
spinedrjxb@sina.com+86 13632494486

Outcome results

None listed

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