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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05159973
Other study ID # 8410
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date October 1, 2021
Est. completion date October 2022

Study information

Verified date November 2021
Source University Hospital, Strasbourg, France
Contact Sébastien HARSCOAT, MD
Phone 33 3 69 15 13 70
Email sebastien.harscoat@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

There are two types of acute coronary syndrome (ACS): ACS with persistent ST segment elevation (ACS ST +) and ACS without ST segment elevation (non-ST + ACS). The incidence of non-ST + ACS is increasing and currently accounts for the majority of myocardial infarction (MI) hospitalizations, while that of ST + ACS is declining. Complications of MI, which include rhythm and conduction disturbances, are mainly associated with ACS ST +. It is recognized that these complications can occur during non-ST + ACS, but with less frequency. This frequency is not clearly established, and has been the subject of few studies. Recent studies in this direction suggest that the frequency of rhythmic complications is low during non-ST + ACS. However, the data collected concerns inter-hospital transport. The aim of the study is to estimate the frequency of occurrence of potentially fatal rhythmic complications in patients admitted to the emergency room and to the cardiology department for non-ST + ACS.


Recruitment information / eligibility

Status Recruiting
Enrollment 500
Est. completion date October 2022
Est. primary completion date October 2022
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - Adult patient (= 18 years old) - Man or woman - Patient admitted to the Emergency Department (SU) or to the Cardiology Department at the NHC between January 1, 2019 and December 31, 2020 - Patient whose main diagnosis retained at the end of hospitalization is a non-ST + ACS - Patient who did not express his opposition to the reuse of his data for scientific research purposes. Exclusion criteria: - Subject having expressed opposition to participating in the study - Subject under guardianship, curatorship or safeguard of justice

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service des Urgences Médico-Chirurgicales Adultes - Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of the frequency of occurrence of potentially fatal rhythmic complications in patients with non-ST segment elevation acute coronary syndrome Files analysed retrospectively from January 01, 2019 to December 31, 2020 will be examined]
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