Cardiomyopathy 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:
- You have been diagnosed with a heart condition called hypertrophic cardiomyopathy (HCM), which means part of your heart wall is thicker than normal (confirm with trial site for exact measurements)
- You are 16 years old or older
- You either do not have an internal heart defibrillator (ICD) device, or you do have one that was fitted as a precaution before any serious heart event occurred
- You are covered by social security insurance (confirm with trial site for specific requirements)
Who may not be able to join:
- Your thickened heart muscle is caused by a specific underlying condition, such as amyloidosis (a protein build-up disease) rather than HCM itself
- You have an internal heart defibrillator (ICD) that was implanted after you already experienced a life-threatening heart event, such as a cardiac arrest or a serious irregular heartbeat
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
Principal Investigator: Philippe CHARRON, MD, PhD, Centre de référence maladies cardiaques héréditaires, Hôpital Ambroise Paré & Hôpital Pitié-Salpêtrière
Phone: + 33 1 49 09 55 43
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
Improvement of the ability to predict major clinical events: C-index comparisons
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.