CTRI/2020/11/028869进行中（未招募）4 期
Postoperative pain relief after laproscopic cholecystectomy: intraperitoneal bupivacaine versus nalbuphine
Hakeem Abdul Centenary hospitalNew Delhi1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2020年5月11日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- to compare and assess the VAS score at different intervals and to determine the time of first analgesic request.
研究概览
简要总结
The aim of the study wasto compare the effectiveness of intraperitoneal bupivacaine and intraperitonealnalbuphine for postoperative pain relief after laproscopic cholecystectomy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Eighty patients ( 40 in each group) with ASA 1,2, aged 18-60 years, undergoing laproscopic cholecystectomy were be included in the study.
排除标准
- •Patients with H/o chronic opioid intake Known allergy to local anaesthetics, Obese or pregnant patients were excluded from the study.
- •Patients those who have chronic pain diseases (not related to choleystitis) or have acute cholecystitis before the surgery were also be excluded When the duration of surgery exceeded 2 hrs or if the surgery got converted to open, were also excluded.
结局指标
主要结局
to compare and assess the VAS score at different intervals and to determine the time of first analgesic request.
时间窗: post operative ,2 ,4 ,6 hrs upto 24 hrs
次要结局
- to compare the analgesic request rate ( number of doses of tramadol in 24 hrs), patient satisfaction score , incidence of shoulder pain and time to return to normal activity.(uptl 24 hrs)
研究者
研究点 (1)
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