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The efficacy and safety of unilateral epidural anesthesia in thoracic surgery——A single-center, randomized, controlled clinical study

The efficacy and safety of unilateral epidural anesthesia in thoracic surgery——A single-center, randomized, controlled clinical study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080351
Enrollment
Unknown
Registered
2024-01-26
Start date
2024-01-27
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

Thoracotomy

Interventions

Epidural anesthesia group:Unilateral epidural anesthesia
General anesthesia group:Paravertebral intercostal nerve block

Sponsors

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Thoracotomy patients, including: esophagus, lung, mediastinum and other diseases. 2. Age 18-75 years old. 3. The ASA classification is in grade I ~ III. 4. There was no history of chronic pain before surgery. 5. Preoperative cardiopulmonary function was normal (NYHA grade ?, EF >50%, FEV1/FVC>70%).

Exclusion criteria

Exclusion criteria: 1. Infection at the puncture site. 2. Combined with central or peripheral neuropathy. 3.The patient has contraindications for surgery, such as serious cardiopulmonary disease and coagulation dysfunction. 4. Senile dementia, cerebral atrophy, acute phase or sequelae of cerebrovascular disease, cognitive impairment. 5. Local or systemic acute infection failed to effectively control. 6. Combined with shock and critical illness, unable cooperate with the operation and effect evaluation. 7. Mental and neurological diseases unable cooperate with the doctor. 8. Patients with a history of allergy to narcotic drugs. 9. Long-term use of opioid analgesics. 10. Chronic alcoholics. 11. Postoperative deterioration and second operation. 12. Other situations in which are inappropriate to participate in the study.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS);

Secondary

MeasureTime frame
Intraoperative ephedrine use;Temporary analgesic drug use;Hemodynamics;Cutaneous sensory change;

Countries

China

Contacts

Public ContactYida Liao, Guangmin Xu

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital

yidaliao@163.com+86 180 8113 8300

Outcome results

None listed

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