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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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04481126
Acronym
COROAKI
Enrollment
168
Registered
2020-07-22
Start date
2020-07-01
Completion date
2022-12-31
Last updated
2021-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Acute Renal Insufficiency

Keywords

Acute Renal Insufficiency, Acute Coronary Syndrome

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.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
incidence of acute renal failureat baselin and at 48 hoursAcute 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

Countries

France

Contacts

Primary ContactPaul GABARRE, MD
paul.gabarre@aphp.fr+33 (0)1 49 09 56 45
Backup ContactEve Vilaine, MD
eve.vilaine@aphp.fr+33 (0)1 49 09 56 45

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026