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:
- Adults aged 18 years or older
- People who have been diagnosed with a specific heart muscle condition called arrhythmogenic right ventricular cardiomyopathy (ARVC), confirmed using recognised medical diagnostic guidelines
- People who are currently being monitored and followed up at the study centre
- People who are able to understand what the study involves and are willing to sign a consent form
Who may not be able to join:
- People who have a history of cancer
- People with severely reduced kidney function
- People with severely reduced liver function
- People who are pregnant or currently breastfeeding
- People who have previously had a specific type of medical imaging scan called a 68Ga-DOTA-SA-FAPI PET/CT scan
- People who are unable or unwilling to sign a written consent form
- People who have any medical, personal, or practical circumstances that the trial doctors believe could interfere with taking part in the study, interpreting the scans, or completing all required follow-up visits (confirm with trial site)
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: +90 555 623 2606
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
Myocardial 68Ga-DOTA-SA-FAPI Uptake on PET/CT
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.