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临床试验/NCT03171688
NCT03171688已完成不适用

Risk Factors for Nausea and Vomiting After Cesarean: Observational Prospective Study

Brasilia University Hospital1 个研究点 分布在 1 个国家目标入组 361 人开始时间: 2016年5月1日最近更新:
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适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
361
试验地点
1
主要终点
Postoperative Nausea or vomiting
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

Investigators will observe the incidence of post-cesarean nausea or vomiting and try to associate it with some risk factors.

详细描述

A single prospective cohort of women submitted to cesarean section who received spinal anesthesia will be assessed for the proposed risk factors and the incidence of nausea or vomiting will be observed during the first 48 hours.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 100 Years（Adult, Older Adult）
性别
Female
接受健康志愿者
否

入选标准

  • •Cesarean section indicated
  • •Spinal anesthesia indicated

排除标准

  • •Cesarean section did not occur
  • •Spinal anesthesia was not provided
  • •Another spinal technique was added to spinal

结局指标

主要结局

Postoperative Nausea or vomiting

时间窗: 48 hours.

The occurrence of postoperative nausea or vomiting, reported by the patient or witnessed by a healthcare provider during the first 48 hours after the cesarean. It is a dichotomic (true or false) outcome.

次要结局

未报告次要终点

研究者

发起方
Brasilia University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Gabriel Magalhaes Nunes Guimaraes

Head of Anesthesiology

Brasilia University Hospital

研究点 (1)

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