Friedreich Ataxia 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
For people with Friedreich's Ataxia (FRDA):
Who might be able to join this trial:
- You are male or female, between 12 and 50 years old
- You are willing and able to give your consent to participate (teenagers will need to give their own agreement, and a parent must also give consent)
- You have a confirmed diagnosis of Friedreich's Ataxia, based on your symptoms and genetic test results
- Your heart's pumping strength (measured by an ultrasound of the heart) is above a certain level — if you haven't had this test recently, it will be done before you join
Who may not be able to join:
- You have signs or symptoms of heart failure
- You have moderate to severe irregular heart rhythms
- You have a history of chest pain caused by reduced blood flow to the heart (angina)
- You have an implanted pacemaker, defibrillator, or any other device that would prevent you from having an MRI scan
- You are on dialysis, have significantly reduced kidney function, or have a sudden kidney injury (if a recent kidney test isn't available, one will be done before your MRI)
- You are pregnant
- You have taken part in a study involving an experimental drug or device recently, or are currently enrolled in one
- You are unable to have a cardiac MRI scan using a special dye (contrast), or you have claustrophobia (fear of enclosed spaces)
- You have been diagnosed with Type 1 or Type 2 Diabetes
- You have any other condition or health issue that the study doctor believes would make it unsafe or unsuitable for you to participate (confirm with trial site)
For healthy volunteers (normal controls):
Who might be able to join this trial:
- You are male or female, between 12 and 30 years old
- You are willing and able to give your consent to participate (teenagers will need to give their own agreement, and a parent must also give consent)
- Your age, gender, and ethnicity are similar to those of participants in the Friedreich's Ataxia group
- You are able to complete the various heart assessment tests involved in the study
- Your heart's pumping strength (measured by an ultrasound of the heart) is above a certain level — if you haven't had this test recently, it will be done before you join
Who may not be able to join:
- The study doctor does not consider you to be in good overall health
- You have signs or symptoms of heart failure
- You have moderate to severe irregular heart rhythms
- You have a history of chest pain caused by reduced blood flow to the heart (angina)
- You have an implanted pacemaker, defibrillator, or any other device that would prevent you from having an MRI scan
- You are on dialysis, have significantly reduced kidney function, or have a sudden kidney injury (if a recent kidney test isn't available, one will be done before your MRI)
- You are pregnant or breastfeeding
- You have taken part in a study involving an experimental drug or device recently, or are currently enrolled in one
- You are unable to sit upright with back support
- You are unable to have a cardiac MRI scan using a special dye (contrast), or you have claustrophobia (fear of enclosed spaces)
- You are unable to take part in exercise tests
- You have been diagnosed with Type 1 or Type 2 Diabetes
- You have any other condition or health issue that the study doctor believes would make it unsafe or unsuitable for you to participate (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
Principal Investigator: Ronald G Crystal, MD, Weill Medical College of Cornell University
Phone: 646-962-5527
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
Level of troponin, BNP, and CPK in blood; echocardiogram; exercise-stress test
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.