临床试验/CTRI/2021/09/036445

CTRI/2021/09/036445尚未招募4 期

Median effective volume of 0.5% ropivacaine for ultrasound guided multiple injection lateral sagittal infraclavicular plexus block: a dose finding study

Post Graduate Institute of Medical Education Research0 个研究点目标入组 0 人开始时间: 待定最近更新: 2021年11月24日

试验速览

阶段: 4 期
状态: 尚未招募
发起方: Post Graduate Institute of Medical Education Research

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型: Interventional

入排标准

入选标准

•Patients with American Society of Anesthesiologists (ASA) physical status I-II patients, in the age group of 18-60 years, with a body mass index (BMI) between 18 and 30 kg.m-2, scheduled to undergo forearm and hand surgeries will be assessed for eligibility

排除标准

•Patients with local infection at the block site, coagulopathy, sepsis, BMI >30, allergy to local anesthetics, uncontrolled hypertension or ischemic heart disease, renal or hepatic dysfunction, pre-existing neurological deficits, prior surgery in the infraclavicular fossa, psychiatric illness, patients who failed to understand the scoring systems used in the study and patients who refused to give consent for the study will be excluded.

研究者

发起方

Post Graduate Institute of Medical Education Research

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