CTRI/2022/04/041666尚未招募不适用
Efficacy of Butorphanol and Tramadol as adjuvant to Levobupivacaine for postoperative analgesia in brachial plexus block- A randomized double blind study
Dr Jaya Lalwani1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年11月4日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Duration of postoperative analgesia
研究概览
简要总结
This is a prospective observational study to see the duration of postoperative analgesia when Butorphanol and Tramadol given with Levobupivacaine for brachial plexus block in patients undergoing below elbow upper limb surgery aged 18 to 65 years with ASA grade I to III. It will be conducted at single centre in India. The primary outcome will be duration of postoperative analgesia and secondary outcomes will be assessment of pain using VAS, onset and duration of sensory and motor blockade and monitoring associated symptoms like allergic reactions, nausea, vomiting, pneumothorax, Horner’s syndrome.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant and Investigator Blinded
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 grade I to III
- •Patients undergoing elective below elbow upper limb surgery under ultra sound guided supraclavicular brachial plexus block.
排除标准
- •Patient refusal
- •Local infection at injection site
- •Failure of block
- •Any bleeding disorder and patient on anticoagulants
- •Allergy to study drugs
- •Severe respiratory, renal and liver disorder
- •Glucose intolerance and diabetic patient
- •Neurological deficit involving brachial plexus
- •Morbidly obese
- •Pregnant women
- •Drug abuse.
结局指标
主要结局
Duration of postoperative analgesia
时间窗: First 24 hours of postoperative period
次要结局
- ⮚ Assessment of pain using VAS(⮚ Onset of sensory and motor blockade)
研究者
研究点 (1)
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