CTRI/2026/03/105656招募中3 期
A double blinded three arm study comparing administration of saline, levobupivacaine, levobupivacaine with dexmedetomidine intraperitoneally to reduce post-operative laparoscopic pain.
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 99
- 试验地点
- 1
- 主要终点
- To compare the postoperative pain scores VAS among patients receiving intraperitoneal levobupivacaine, levobupivacaine with dexmedetomidine and normal saline.
研究概览
简要总结
To compare the postoperative pain scores VAS among patients receiving intraperitoneal levobupivacaine, levobupivacaine with dexmedetomidine and normal saline.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •1.ASA grade -I 2.ASA grade-II 3.Age group between 18 and 70 years undergoing laparoscopic procedure.
排除标准
- •Previous history of allergies to the study drug.
结局指标
主要结局
To compare the postoperative pain scores VAS among patients receiving intraperitoneal levobupivacaine, levobupivacaine with dexmedetomidine and normal saline.
时间窗: 24 hours
次要结局
- -To measure the duration of analgesia provided by 0.9% normal saline ,0.5% levobupivacaine, 0.5% levobupivacaine with 1mcg/kg dexmedetomidine.(-To measure the total doses of analgesic (opioid) consumption in each group.)
研究者
Lijoe Reuben
Pondicherry Institute of medical sciences
研究点 (1)
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