CTRI/2019/05/019341尚未招募1/2 期
A prospective randomized controlled trial to compare the efficacy and safety of different doses of clonidine when used as an adjuvant to intrathecal bupivacaine
J J hospital1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2019年1月6日最近更新:
试验速览
- 阶段
- 1/2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- Block height
研究概览
简要总结
Spinal anesthesia has been the technique of choice for lower limb and abdominal surgeries and is preferred over general anesthesia. Many adjuvants have been studied to prolong the duration of action of spinal anesthesia. In our study we would like to study the effects of adding different doses of clonidine as a adjuvant to bupivacaine in subarachnoid block and observe the effects and adverse events
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- All
入选标准
- •ASA I or II normotensive patients undergoing elective orthopaedic surgery.
排除标准
- •ASA III & above, patients with cardiovascular, renal, liver dysfunction, allergy to clonidine or bupivacaine, short height (<130cm), obese(BMI > 30kg/m2) or with contraindication to spinal.
结局指标
主要结局
Block height
时间窗: 1year
Duration of analgesia/sensory block
时间窗: 1year
Hemodynamic variations-pulse, MAP
时间窗: 1year
Complications
时间窗: 1year
次要结局
- Hemodynamic effects-pulse and MAP(Complications)
研究者
研究点 (1)
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