临床试验/CTRI/2024/08/071945

CTRI/2024/08/071945尚未招募不适用

Comparison of intrathecal morphine and adductor canal block for analgesic efficacy in patients undergoing knee arthroplasty-a randomized controlled study

Aiims Kalyani1 个研究点分布在 1 个国家目标入组 80 人开始时间: 2024年8月13日最近更新: 2024年8月2日

试验速览

阶段: 不适用
状态: 尚未招募
发起方: Aiims Kalyani
入组人数: 80
试验地点: 1
主要终点: Cumulative morphine equivalent 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 study we compare intrathecal morphine and adductor canal block for analgesic efficacy in patients undergoing knee arthroplasty by measuring 24 hours cumulative morphine equivalent consumption and also by measuring postoperative pain score by numerical rating scale

研究设计

研究类型: Interventional
分配方式: Randomized
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

•Adult patients of Age 18-65 years of both sexes with American Society of Anesthesiologist (ASA) 1 and 2 undergoing knee arthroplasty under spinal anesthesia.

排除标准

•total surgical duration more than 3 hours ASA 3 and 4 refuse to consent for spinal anesthesia history of coagulopathy with raised INR more than or equal to 1.5 local infection at needle insertion site history of psychiatric illness and on antipsychotic medications history of opioid dependence history of chronic pain.

结局指标

主要结局

Cumulative morphine equivalent consumption

时间窗: 24 hours

次要结局

1.Numeric Rating scale for pain(2. Time to first postop mobilisation)

研究者

发起方

Aiims Kalyani

申办方类型

Research institution and hospital

责任方

Principal Investigator

主要研究者

Dr.Jaipriya Desigan

Aiims,Kalyani

研究点 (1)

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