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临床试验/NCT05992961
NCT05992961已完成不适用

The Effects of Troponin I Surveillance Among Patients Undergoing Acute High-risk Abdominal Surgery

Nordsjaellands Hospital1 个研究点 分布在 1 个国家目标入组 558 人开始时间: 2018年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
558
试验地点
1
主要终点
compare the mortality rate before and after implementing troponin I surveillance

研究概览

简要总结

Treatment of disorders such as gastrointestinal tract (GI) perforation, ischemia and obstruction often require acute high-risk abdominal surgery, which is associated with a high risk of complications such as myocardial injury after non-cardiac surgery (MINS) and mortality. The majority of patients with MINS will not experience any symptoms, and thus MINS remains undetected without routine troponin measurements.

The investigators hypothesized that implementing surveillance with troponin I as a standard care might be useful as risk stratification, and that increased surveillance, examinations, and subsequent individually based medical interventions, might improve the outcomes for patients with MINS.

研究设计

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

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

  • Eligible patients were 18 years or older
  • Undergoing surgery for gastrointestinal perforation, obstruction, mesenterial ischemia or necrosis, or anastomotic leakage.

排除标准

  • Not undergoing surgery for one of the conditions above

结局指标

主要结局

compare the mortality rate before and after implementing troponin I surveillance

时间窗: 30-, 90-, and 365-day

compare the 30-, 90-, and 365-day mortality rate after acute hugh-risk abdominal surgery in patients undergoing postoperative troponin I surveillance and subsequent intervention with a historical group of patients not undergoing troponin I surveillance.

次要结局

未报告次要终点

研究者

发起方
Nordsjaellands Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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