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临床试验/NCT04889534
NCT04889534已完成不适用

Evaluation of Predictive Factors for Nausea, Vomiting and Postoperative Acute Pain in Oncological Patients

Instituto do Cancer do Estado de São Paulo1 个研究点 分布在 1 个国家目标入组 1,500 人开始时间: 2015年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,500
试验地点
1
主要终点
Intensity of postoperative pain

研究概览

简要总结

1809 patients were evaluated in postoperative period. They were asked about nausea, vomiting, retching and pain in the first postoperative 24 hours

详细描述

Patients were prospectively evaluated , and nausea, vomiting and pain were recorded.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients submitted to oncological surgeries

排除标准

  • refusal to sign the agreement term
  • lack of information in the records

结局指标

主要结局

Intensity of postoperative pain

时间窗: 24 hours

pain intensity was measured using descriptive and verbal number scale

次要结局

  • side effects from analgesia(24 hours)

研究者

发起方
Instituto do Cancer do Estado de São Paulo
申办方类型
Other
责任方
Sponsor

研究点 (1)

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