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NCT07112547: SurvSCA

Occurrence of Severe Cardiac Rhythm and Conduction Disturbances in Emergency Department Patients With Non-ST Elevation Acute Coronary Syndrome

Not yet recruiting Last updated 8 August 2025
What this trial tests

trial in Acute Coronary Syndrome Without ST Elevation on Electrocardiogram in 500 participants. Not yet recruiting.

Timeline
1 September 2025
Primary endpoint
1 October 2028
1 October 2028

Quick facts

Lead sponsorUniversity Hospital, Strasbourg, France
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment500
Start date1 September 2025
Primary completion1 October 2028
Estimated completion1 October 2028
Sites10 locations across France

Conditions studied

Sponsor

University Hospital, Strasbourg, France

Who can join

18 and older, any sex, with Acute Coronary Syndrome Without ST Elevation on Electrocardiogram or Acute Coronary Syndromes (ACS). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Cardiovascular diseases are the leading cause of death worldwide. Among them, coronary artery disease-especially in its acute form, known as acute coronary syndrome (ACS)-is the most frequent cause of cardiovascular death. There are two main types of ACS: ST-segment elevation myocardial infarction (STEMI) and non-ST-segment elevation ACS (NSTE-ACS). While the occurrence of serious heart rhythm and conduction disturbances is well established in STEMI, these complications are believed to be much less frequent in NSTE-ACS. However, their actual frequency in this population remains unclear due to limited studies, especially in emergency settings. The main purpose of this study is to estimate the frequency of serious rhythm and conduction disorders in patients presenting with NSTE-ACS in emergency departments. The hypothesis is that these events are rare in this population and may not justify routine continuous cardiac monitoring for all such patients, as currently recommended. Secondary objectives include identifying risk factors for these complications, estimating their frequency during hospitalization, assessing the frequency of minor rhythm and conduction disorders, evaluating care times and patient flow in emergency departments, and assessing patient outcomes up to 30 days-including hospitalizations, length of stay, discharge disposition, all-cause mortality, and the occurrence of five major adverse cardiovascular events (5-point MACE).

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Trials by the same sponsor.

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Data sources for this page

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