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临床试验/CTRI/2021/02/031464
CTRI/2021/02/031464已完成未知

Comparison of efficacy and safety of 2chloroprocaine 1 percent with hyperbaric bupivacaine 0.5 percent in subarachnoid block for cesarean section - ChlorprocaineCS

Dr SUJEET RAI0 个研究点目标入组 96 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
96

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

  • Pregnant Female patients aged between 18-35 years undergoing elective caesarean section of American society of anaesthesiology (ASA) physical status I and II and giving consent will be included.

排除标准

  • Patient refusal or uncooperative patients, Patients with severe cardiopulmonary disease, allergy or intolerance to local anaesthetics, coagulation disorders, neurologic disease or spine deformities, Infection at the site of needle insertion, of ASA physical status 3 and 4 will be excluded.

研究者

发起方
Dr SUJEET RAI

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