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NCT07545512Recruiting

ODSSEY-SCD_Identification Of Markers to preDict the rISk of Sudden Cardiac Death in Moderated LVEF in ischEmic cardiomyopathY

ODISSEY-SCD_Identification Of Markers to preDict the rISk of Sudden Cardiac Death in Moderated LVEF in ischEmic cardiomyopathY (ODISSEY-SCD

Source: ClinicalTrials.gov · Last updated 28 Oct 2026

Brief summary (registry, in English)

Although advances in treatment and patient management have considerably improved post-infarction prognosis, the risk of sudden cardiac death remains a major concern. Sudden cardiac death (SCD) is defined as an unexpected death occurring within one hour of the onset of symptoms, often of arrhythmic origin. In patients who have survived a myocardial infarction, sudden death represents a persistent threat. This risk is often associated with complications such as left ventricular dysfunction, malignant ventricular arrhythmias, and structural alterations of the myocardium, all of which can favor the development of fatal cardiac events. Among the risk factors identified, reduced left ventricular ejection fraction, a history of ventricular arrhythmias and the presence of extensive scarring of the myocardium are particularly significant. Assessing the risk of SCD in post-infarction patients is crucial to determining appropriate prevention strategies, such as implanting automatic implantable defibrillators (ICDs). Assessment tools are varied, but currently only left ventricular ejection fraction (LVEF) \< 35% is identified and validated. However, this risk stratification is unsatisfactory, particularly in view of SCD in patients with a history of myocardial infarction and a moderately impaired LVEF (between 35 and 50%). Although the initial treatment of myocardial infarction is essential for the patient's immediate survival, managing the risk of sudden death in the long term remains a major clinical challenge. A multiparametric approach is needed to optimize prognosis and prevent premature death in these patients.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
400 (estimated)
First submitted
13 Mar 2026
Start date
1 Oct 2026
Primary completion date
1 Jul 2033
Lead sponsor
University Hospital, Clermont-Ferrand
NCT number
NCT07545512

What you commit to

  • Study type: Interventional
  • Planned participants: 400
  • From 1 Oct 2026 to the primary completion date, 1 Jul 2033
  • 15 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Administration of ventricular antiarrhythmic drugs other than beta-blockers (i.e. amiodarone, sotalol, flecainide)
  • Patient participating in another clinical research protocol involving an investigational drug or device within the last 30 days (participation in a registry is permitted at the same time).

Other illness

  • Patients with systemic diseases (cancer, liver failure or end-stage renal disease)

Age

  • Age \> 80
  • The subject is pregnant or nursing or positive beta HCG for women of childbearing age

Other

  • Presence of a secondary prevention indication for implantation of an implantable automatic defibrillator (ICD)
  • Presence of a pacemaker
  • Patients with assessed life expectancy \< 1 year.
  • Adult patient under legal protection (guardianship, curatorship or other legal protection measure)

Who the study is looking for

  • Patients over 18 years of age
  • Hospitalized for acute STEMI within 6 months (Type 1 myocardial infarction according to ESC recommendations, Thygesen EHJ 2018).
  • Left ventricular ejection fraction between 35% and 50% at least 40 days after acute myocardial infarction (see above).
  • Under optimal tolerated medical treatment.
  • Covered by a social security scheme.
  • Legally competent to give voluntary informed consent to participate in the study.
  • Patient who will not participate in further studies involving an investigational drug or device until the end of the trial (i.e. 60 months). Participation in registries is authorized

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Amiens
Coordinator of this site? Confirm its status
AmiensFranceNot yet recruiting
Chu Brest
Coordinator of this site? Confirm its status
BrestFranceNot yet recruiting
CHU Caen
Coordinator of this site? Confirm its status
CaenFranceNot yet recruiting
CHU Clermont-Ferrand
Coordinator of this site? Confirm its status
Clermont-FerrandFranceNot yet recruiting
CHRU Lille
Coordinator of this site? Confirm its status
LilleFranceRecruiting
HCL - Hôpital de la Croix Rousse
Coordinator of this site? Confirm its status
LyonFranceNot yet recruiting
HCL - Hôpital Pierre Wertheimer
Coordinator of this site? Confirm its status
LyonFranceNot yet recruiting
CHU Nancy
Coordinator of this site? Confirm its status
NancyFranceNot yet recruiting
CHU Nantes - Hopital Nord Laënnec
Coordinator of this site? Confirm its status
NantesFranceRecruiting
APHP Hôpital Européen Georges Pompidou
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
CHU de Poitiers
Coordinator of this site? Confirm its status
PoitiersFranceNot yet recruiting
CHU Saint-Etienne
Coordinator of this site? Confirm its status
Saint-EtienneFranceNot yet recruiting
CHU Strasbourg
Coordinator of this site? Confirm its status
StrasbourgFranceRecruiting
CHU Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceNot yet recruiting
CH Vichy
Coordinator of this site? Confirm its status
VichyFranceNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.