Comparative Study of Efficacy of Palonosetron 0.25mg versus 0.125mg Palonosetron Plus 4mg Dexamethasone in Prevention of Post Operative Nausea and Vomiting in Patients Undergoing Laparoscopic Cholecystectomy - NIL

Md Zamal Ahmad0 个研究点目标入组 120 人开始时间: 2026年7月29日最近更新: 2026年8月3日

干预措施

试验速览

阶段: 4 期
状态: 进行中（未招募）
发起方
入组人数: 120

研究概览入排标准研究组 & 干预措施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

•Age group between 18 to 60 years of both sexes having ASA status I and II undergoing elective laparoscopic cholecystectomy and willing to give informed written consent

排除标准

•Patients unwilling to participate, Patients with history of post operative nausea and vomiting or motion sickness, gastrointestinal motility disorders, hypersensitivity to study drugs, patients on drugs causing nausea and vomiting, diabetes mellitus, ear disease.

研究组 & 干预措施

Intervention1: Palonosetron 0.125mg plus Dexamethasone 4mg: Palonosetron 0.125mg intravenous plus Dexamethasone 4mg intravenous administered just before induction of anaesthesia in patients undergoing laparoscopic cholecystectomy under general anaesthesia. Total sample size in this group will be 60 patients.

干预措施: Intervention1: Palonosetron 0.125mg plus Dexamethasone 4mg: Palonosetron 0.125mg intravenous plus Dexamethasone 4mg intravenous administered just before induction of anaesthesia in patients undergoing laparoscopic cholecystectomy under general anaesthesia. Total sample size in this group will be 60 patients.

研究者

发起方

Md Zamal Ahmad

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