CTRI/2017/05/008664尚未招募未知
A randomised control trial to evaluate the efficacy and safety of port site and intraperitoneal infiltration of bupivacaine for reducing post operative pain in laparoscopic gynaecological surgeries - NI
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 入组人数
- 100
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
入选标准
- •ASA status I & II
- •All cases of Operative laparoscopic gynaecological surgeries
排除标准
- •Laparoscopic Gynaecological Oncology surgeries
- •history of opiod use/ alcohol abuse in last 24 hours prior to study
- •Weight < 50kg
- •history of allergy to the drug in study
- •Chronic Pain Syndrome
研究者
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