CTRI/2023/07/055456尚未招募不适用
Comparison of analgesic efficacy of wound infiltration with bupivacaine versus bupivacaine and tramadol for postoperative pain relief in lower segment cesarean section under spinal anesthesia
Dr D Y Patil Medical college and hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年1月9日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Observe analgesic Efficacy of Wound Infiltration with Bupivacaine for Postoperative Pain Relief in Lower Segment Caesarean Section under Spinal Anaesthesia
研究概览
简要总结
It is a randomized prospective comparative double blind study where in Comparison of Analgesic Efficacy of Wound Infiltration with Bupivacaine versus Bupivacaine and Tramadol for Postoperative Pain Relief in Lower Segment Caesarean Section under Spinal Anaesthesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant, Investigator and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 35.00 Year(s)(—)
- 性别
- Female
入选标准
- •ASA Grade I or II fit patients.
- •1.Pregnant women age between 18 to 35 years undergoing Lower Segment Cesarian Section under spinal anesthesia.
- •2.Hemodynamically stable patients with all routine investigations within normallimits without any other co- morbidities.
排除标准
- •Severe cardiopulmonary, renal or liver disease 1.Preeclampsia & Eclampsia 2.Allergy to tramadol or bupivacaine 3.Patient refusal 4.Patient with ASA Grade III or > III.
- •5.Patients with drug allergy.
结局指标
主要结局
Observe analgesic Efficacy of Wound Infiltration with Bupivacaine for Postoperative Pain Relief in Lower Segment Caesarean Section under Spinal Anaesthesia
时间窗: Postoperative at 2 hours,4 hours, 6 hours, 12 hours, 24 hours
次要结局
- Observe analgesic Efficacy of Wound Infiltration with Bupivacaine plus tramadol for Postoperative Pain Relief in Lower Segment Caesarean Section under Spinal Anaesthesia(Postoperative at 2 hours, 4 hours, 6 hours, 12 hours, 24 hours)
研究者
研究点 (1)
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