TCTR20211013003Enrolling By Invitation4 期
Comparison of efficiency of preoperative single dose tramadol/paracetamol combination between 50/500 VS 75/650 mg on acute postoperative pain after abdominal gynecologic surgery: a randomized controlled trial
适应症
试验速览
- 阶段
- 4 期
- 状态
- Enrolling By Invitation
- 入组人数
- 74
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. 18-65 year old women, 2. ASA physical status classification 1-2, 3. undergoing open abdominal benign gynecologic condition
排除标准
- •1. History of study drug allergy, 2. History of chronic pain, liver disease or gastrointestinal bleeding, 3. pregnancy, 4. psychiatric problem
研究者
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