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Assessment of perioperative analgesia and comfort in patients with percutaneous endoscopic lumbar discectomy with thoracolumbar interfascia plane block

Assessment of perioperative analgesia and comfort in patients with percutaneous endoscopic lumbar discectomy with thoracolumbar interfascia plane block

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055671
Enrollment
Unknown
Registered
2022-01-16
Start date
2022-01-17
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Lumbar Disc Protrusion

Interventions

Group 1 :Nothing
Group 2:Thoracolumbar Interfascial Plane Block and Compound Betamethasone Injection
Group 3:Thoracolumbar Interfascial Plane Block and Ropivacaine

Sponsors

The First Affiliated of AnHui Medical University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Select patients undergoing percutaneous endoscopic lumbar discectomy at the selected stage, aged 18-80 years, with no gender restrictions; 2. American Society of Anesthesiologists (ASA) Grades I and II; 3. Body mass index (BMI) 18- 24 kg/m2.

Exclusion criteria

Exclusion criteria: 1. Serious respiratory and circulatory diseases: such as severe coronary heart disease, COPD, etc.; 2. Diseases of the endocrine system: pituitary tumor, severe diabetes, hypercortisol signs, pheochromocytoma, etc.; 3. Sinus bradycardia or AV block; 4. History of allergy to anesthetics; 5. Infection at the site of the puncture; 6. Mental illness such as schizophrenia, depression, history of chronic analgesic drugs, history of alcoholism, opioid dependence or inability to understand visual analogue scale (VAS); 7. History of bleeding disorders or abnormal coagulation function; 8. Anxious or depressed patients; 9. Pregnant women or maternity; 10. Patients with recurrence of lumbar disc herniation; 11. Situations where other investigators find inappropriate for this study.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS) score;The 15-Item Quality of Recovery score scale;The Oswestry Disability Index;

Secondary

MeasureTime frame
Perioperative hemodynamics;Operation time;Postoperative hospital stay;

Countries

China

Contacts

Public ContactWang Likui

Graduate School of AnHui Medical University

wlk9560@163.com+86 13705690702

Outcome results

None listed

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