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临床试验/NCT03141645
NCT03141645已完成不适用

Comparison of Preoperative Intravenous Fluid Loading and Ondansetron in Reduction of Incidence Postoperative Nausea and Vomiting After Laparoscopic Cholecystectomy: A Prospective Randomized Controlled Study

Siriraj Hospital1 个研究点 分布在 1 个国家目标入组 171 人开始时间: 2017年6月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
171
试验地点
1
主要终点
The incidence of postoperative nausea and vomiting

研究概览

简要总结

This study is designed to examine the incidence of postoperative nausea and vomiting during 24 hours after elective laparoscopic cholecystectomy in patients receiving preoperative intravenous fluid loading (group F), ondansetron (group O) and receiving neither fluid nor ondansetron or control group (group C).

详细描述

This study is a prospective randomized control trial. It is designed to examine the incidence of postoperative nausea and vomiting during 24 hours after elective laparoscopic cholecystectomy in patients receiving preoperative intravenous fluid loading (group F), ondansetron (group O) and receiving neither fluid nor ondansetron or control group (group C). This study is hypothesized that the incidence of PONV in patients receiving preoperative intravenous fluid loading (group F) and patients receiving ondansetron (group O) will be similarly reduced from the control group (receiving neither fluid nor ondansetron).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with aged 18 to 70 years with an ASA physical status 1-3
  • Exclusion Criteria including patients
  • with pregnant or breast-feeding patients
  • having history of taking antiemetic drugs within 24 hours before surgery
  • with hypersensitivity or allergy to ondansetron
  • with CKD stage 4, 5
  • with congestive heart failure, LVEF <40
  • with cirrhosis child c
  • refusal or cannot communicate or understand the purpose of this study

排除标准

  • 未提供

研究组 & 干预措施

Fluid loading group

Experimental

Patients will receive ringer lactate solution 10ml/kg in 15 minutes before starting operation

干预措施: Fluid loading (Other)

Ondansetron group

Active Comparator

Patients will receive an 8 mg of intravenous ondansetron in 15 minutes before finishing operation.

干预措施: Ondansetron (Drug)

结局指标

主要结局

The incidence of postoperative nausea and vomiting

时间窗: 24 hours

The incidence of postoperative nausea and vomiting within postoperative 24 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mingkwan Wongyingsinn, MD

Assistant Professor

Siriraj Hospital

研究点 (1)

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