TCTR20240708004尚未招募3 期
Efficacy of intravenous lidocaine infusion for postoperative quality of recovery in laparoscopic gynecological surgery : A triple-blind, randomized controlled trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 64
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 65 Years（—）
- 性别
- Female
入选标准
- •1. Patients who scheduled for elective laparoscopic gynecological surgery for benign diseases
- •2. ASA physical status 1-2
排除标准
- •1. Pregnancy
- •2. Body weight < 40 kg or BMI > 35 kg/m2
- •3. History of local anesthetic allergy
- •4. History of cardiac arrhythmia
- •5. Cirrhosis or elevated AST or ALT >/= 2x of normal upper limit
- •6. GFR </= 60 ml/min/1.73m2
- •7. Neurological disease
- •8. NSAID or sulfa drugs allergy
- •9. History of GI bleeding or peptic ulcer
- •10. Regular use of analgesics
- •11. Unable to fully understand Thai and access questionnaire and pain rating
研究者
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