CTRI/2020/02/023167已完成不适用
Comparing different doses of dexmedetomidine combined with ropivacaine for ultrasound guided supraclavicular brachial plexus block in upper limb surgeries - A prospective randomised control trial
P Akshara1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2020年10月2日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- To compare duration of analgesia of two different doses of dexmedetomidine in terms of first rescue analgesia requirement
研究概览
简要总结
This is a randomized controlled trial to compare the efficacy of different doses of Dexmedetomidine when combined with Ropivacaine in supraclavicular brachial plexus block among 50 patients posted for upper limb surgeries over a period of 18 months. The primary objective is to compare the duration of analgesia post-operatively. The secondary outcomes are to assess the onset and duration of sensorimotor block, peri operative analgesic requirement, sedation score and hemodynamic stability.
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
- •Patients undergoing elective upper limb surgeries American Society of Anaesthesiologist I or II.
排除标准
- •Patient refusal Patients with pre existing peripheral neuropathy of upper limb Patients allergic to local anesthetics Patients on adrenoreceptor agonist/ antagonist therapy American Society of Anaesthesiologist III and above Patients with coagulation disorders Local site infection BMI above 30 Poorly controlled Hypertension Poorly controlled Diabetes mellitus Severe CVS abnormalities Renal/Hepatic insufficiency Pregnancy/ Lactating mothers.
结局指标
主要结局
To compare duration of analgesia of two different doses of dexmedetomidine in terms of first rescue analgesia requirement
时间窗: Post operative period
次要结局
- Onset and duration of sensorimotor blockade(Peri operative analgesic requirements)
研究者
研究点 (1)
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