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CMR Imaging Techniques for Heart Disease (Myomapping Trial)
N/A
Recruiting
Led By Joseph U. Schoepf, MD
Research Sponsored by Medical University of South Carolina
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Subject must be previously diagnosed with or suspected to have one of the following conditions: Myocardial ischemia or infarction (group 1), Hypertrophic cardiomyopathy (group 2), Infiltrative cardiomyopathy (group 3), Myocarditis (group 4).
Subject must be 18-90 years of age.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial will test if a new MRI technique can help diagnose and treat patients with heart conditions.
Who is the study for?
This trial is for adults aged 18-90 with suspected or diagnosed heart conditions like ischemic heart disease, hypertrophic cardiomyopathy, infiltrative cardiomyopathy, or myocarditis. They must be referred for a CMR scan and can't participate if they have metal implants, acute psychiatric disorders, substance abuse issues, allergies to MRI contrast agents, are in an unstable condition or won't follow the study rules.
What is being tested?
The trial is testing advanced Cardiac Magnetic Resonance Imaging (CMR) techniques to better diagnose and monitor various heart diseases. It aims to see how well these new fast quantitative imaging methods work compared to traditional ones.
What are the potential side effects?
Since this trial involves imaging techniques rather than drugs, side effects may include discomfort during the procedure or reactions to contrast agents used in some MRIs such as mild allergic reactions.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check βYesβ for the criteria belowSelect...
I have or might have a heart condition such as blocked arteries, thickened heart muscle, a disease causing heart tissue buildup, or inflammation of the heart muscle.
Select...
I am between 18 and 90 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Additional 5 minute research MR scan of heart.Experimental Treatment1 Intervention
The purpose of this is to evaluate new, faster MR scans
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Who is running the clinical trial?
Medical University of South CarolinaLead Sponsor
968 Previous Clinical Trials
7,399,018 Total Patients Enrolled
Joseph U. Schoepf, MDPrincipal InvestigatorMedical University of South Carolina
1 Previous Clinical Trials
149 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I have or might have a heart condition such as blocked arteries, thickened heart muscle, a disease causing heart tissue buildup, or inflammation of the heart muscle.I am between 18 and 90 years old.You are currently using or dependent on drugs or alcohol.You must have been referred for a needed heart imaging test.
Research Study Groups:
This trial has the following groups:- Group 1: Additional 5 minute research MR scan of heart.
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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