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

Conditions
Acute Renal Insufficiency
Acute Coronary Syndrome
Registration Number
NCT04481126
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
168
Inclusion Criteria
  • 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.
Exclusion Criteria
  • 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.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
incidence of acute renal failureat 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

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Nephrology department, Ambroise Paré hospital, APHP

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Boulogne-Billancourt, France

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