A prospective, randomized, single blinded study to compare analgesic efficacy of pectointercostal fascial block and erector spine block in patients undergoing cardiac surgery- a pilot study

NA1 个研究点分布在 1 个国家目标入组 30 人开始时间: 2021年6月22日最近更新: 2021年5月12日

试验速览

阶段: 不适用
状态: 已完成
发起方
入组人数: 30
试验地点: 1
主要终点: total opioid consumption

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

In this prospective randomized study patients undergoing cardiac surgery through sternotomy will be recruited and randomized to receive either pectointercostal fascial block or erector spine block bilateral and there analgesia efficacy will be compared after surgery

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 70.00 Year(s)（—）
性别: All

入选标准

•Adult (more than 18 years) Undergoing cardiac surgery with midline sternotomy Haemodynamically stable Elective surgery Extubation within 3 hrs of performing block.

排除标准

•Hemodynamic instability (left ventricular ejection fraction <30%, on ventricular assist device) Aortic surgery Emergency surgery Minimally invasive procedures.

结局指标

主要结局

total opioid consumption

时间窗: 24hrs after surgery

次要结局

pain at rest(pain on deep breathing)

研究者

发起方

申办方类型

Other [nil]

研究点 (1)

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