CTRI/2021/08/035730尚未招募1 期
TO ASSESS THE ANALGESIC EFFICACY OF ORAL CLONIDINE VS INTRATHECAL CLONIDINE ADDED AS AN ADJUVANT TO 0.5% HYPERBARIC BUPIVACAINE IN CESAREAN SECTION --- A PROSPECTIVE RANDOMIZED DOUBLE BLIND CONTROLLED TRIAL.
Dr Vignesh T M1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年8月20日最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- To determine the duration of analgesia.
研究概览
简要总结
This study is a randomized single centre trial comparing the effect of Intrathecal clonidine vs oral clonidine when added as an adjuvant to 0.5% hyperbaric bupivacaine in patients undergoing cesarean section, that will be conducted in a single centre in india. The primary objective is to measure the duration of analgesia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 31.00 Year(s)（—）
- 性别
- Female
入选标准
- •ASA physical status â… and â…¡.
- •Age 18-31 years.
- •Singleton pregnancy Informed, written and valid consent.
排除标准
- •Obstetric complications such as Placenta previa, Abruptio placenta and Preeclampsia.
- •Spinal deformity such as kyphoscoliosis.
- •BMI greater than 35kg/m
- •Height less than 150 cm or greater than180 cm.
- •Women with Hypertensive disorders,Cardiovascular disorders,Deep vein thrombosis.
- •Allergy to study drugs.
结局指标
主要结局
To determine the duration of analgesia.
时间窗: Duration of analgesia is assessed every 15 minutes from onset of sensory block to first request for rescue analgesic or VAS score 4 or more.
次要结局
- Onset and duration of sensory block.(Onset and duration of motor block.)
研究者
研究点 (1)
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