Heart Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Adults over 18 years of age.
- People who have had their first heart attack of a specific type (called an ST-segment elevation myocardial infarction) while already in hospital.
- People who have had a procedure to examine their heart's arteries (called a coronary angiography) within 72 hours of the heart attack.
- People who are enrolled in a specific heart attack patient registry called RIMA.
- People who are covered by a social security (health insurance) scheme and have signed a consent form agreeing to take part.
Who may not be able to join:
- People who are already enrolled in this study.
- People who do not have a sufficient understanding of the French language.
- Women who are pregnant, breastfeeding, or who have recently given birth.
- People who are detained or restricted in their freedom by a court or government authority, or who are receiving psychiatric treatment under compulsion (against their will).
- People who are under a legal protection order, or who are not able to give their own informed consent to participate.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 02 41 35 36 37
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Asses left ventricular remodeling disparities between genders
Can't join this trial?
Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.