Comparative study between 0.125 % Bupivacaine and 0.2 %Ropivacaine in Ultrasound Guided Supraclavicular Brachial Plexus Block using PerineuralCatheter for Postoperative Analgesia in Upper limb Surgeries

Dr Syed Arafath Ahmed1 个研究点分布在 1 个国家目标入组 60 人开始时间: 2020年6月15日最近更新: 2021年12月4日

试验速览

阶段: 不适用
状态: 招募中
发起方
入组人数: 60
试验地点: 1
主要终点: To assess the duration of postoperative analgesia using Visual Analogue Scale (VAS) in both groups Group R (Ropivacaine) and Group B (Bupivacaine).

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The proposed study is tocompare the effectiveness of two different local anaesthetic drugs (0.125%Bupivacaine and 0.2% Ropivacaine) in the Post- operative Period after anelectively posted Upper Limb Surgery in patients satisfying the inclusion andthe exclusion criteria

研究设计

研究类型: Interventional
分配方式: Computer generated randomization
盲法: Participant 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

•American Society of Anaesthesiologists(ASA) 1 and 2 Body Weight.

排除标准

•Age less than 18years and age more than 65 years.
•Pregnant women Infection at the site of block Patients with coagulopathy History of allergy to local anaesthetic drugs Mental incapacity or language barrier precluding to informed consent Patient refusal Pre existing motor or sensory deficit in the operative limb Severe pulmonary pathology.

结局指标

主要结局

To assess the duration of postoperative analgesia using Visual Analogue Scale (VAS) in both groups Group R (Ropivacaine) and Group B (Bupivacaine).

时间窗: 1.5 years

次要结局

To assess the degree of motor blockade in both groups(1.5 years)
To assess the time of first rescue analgesia required(1.5 years)

研究者

发起方

Dr Syed Arafath Ahmed

申办方类型

Other [self]

研究点 (1)

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