跳至主要内容
临床试验/NCT04481126
NCT04481126Unknown不适用

Acute Renal Insufficiency (ARI) Rate and Predictive Score of ARI in Hospitalized Patients for Acute Coronary Syndrome With ST-segment Elevation Needing Urgent Coronarography

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 168 人开始时间: 2020年7月1日最近更新:
适应症

试验速览

阶段
不适用
入组人数
168
试验地点
1
主要终点
incidence of acute renal failure

研究概览

简要总结

The primary objective of the study aims to evaluate frequence of acute renal insufficiency in patients with ST-segment elevation who need urgent coronary angiography in Ambroise Paré hospital.

The secondary objectives are:

  • identify factors of risks associated with the occurrence of acute renal insufficiency after coronarography.
  • establish a preprocedure score, predicting of acute renal insufficiency after urgent coronary angiography in patients with ST+ acute coronary syndrome.

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

  • patient aged ≥ 18 years;
  • evocative symptoms of myocardiac ischemia: typical chest pain; ST-segment elevation and 1 mm in two consecutive peripheral leads and 2 mm in two consecutive precordial derivations, or appearance of a bloc of left branch of novo;
  • need urgent coronarography;
  • Covered by french social security scheme included CMU.

排除标准

  • dialysed patient for chronic renal insufficiency;
  • cardio-resporatory arrest;
  • cardiogenic choc state;
  • prior emergency passage to hospital;
  • patient under tutor, gardianship;
  • patient covered by french AME scheme;
  • pregnant women or breastfeeding;
  • all medical, psychological or social situation which should influents the compliance to protocol according to investigator;
  • patient refusal.

结局指标

主要结局

incidence of acute renal failure

时间窗: at baselin and at 48 hours

Acute renal failure is defined as an increase in plasma creatinine of at least 26.5µmol/l within 48 hours, or an increase in plasma creatinine of at least 1.5 times plasma creatinine within 48hours of hospitalisation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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