TCTR20240319003尚未招募3 期
A Randomized Controlled Trial Comparing Dual Subsartorial Block and Adductor Canal Block for Pain Control in Ambulatory Arthroscopic Knee Surgery
ADepartment of Anesthesiology, Faculty of Medicine Ramathibodi Hospital, Mahidol University0 个研究点目标入组 54 人开始时间: 2024年3月19日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 54
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
- 25 Years 至 55 Years（—）
- 性别
- All
入选标准
- •Patients aged between 25 and 55 years.
- •Bodyweight > 40 kg
- •BMI between 18 - 35 kg/m
- •ASA physical status of I or II
- •Written informed consent obtained from the patients, stating I appreciate the opportunity to participate in this study, along with their signature.
排除标准
- •Adults who are unable to provide their own consent.
- •Pre-existing lower extremities weakness
- •Patients who show signs of infection at the site of the block
- •BMI>35kg/m2
- •Allergy or contraindication to any drug used in this study
- •Coagulopathy (assessed through medical history and physical examination, and if clinically necessary, through blood tests, e.g., platelet count =< 100,000 cells/mm3, INR >= 1.4)
- •Chronic pain syndromes requiring the use of chronic opioids
- •History of kidney impairment (estimated GFR < 60ml/min)
- •History of liver dysfunction (history of cirrhosis, portal hypertension or variceal bleeding, AST, ALT >= 50 IU/L)
- •Refusal to participate or withdrawal of consent at any stage of the study
研究者
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