Creation of an ECG Database in 3T MRI With Healthy Heart and Several Kind of Cardiac Disease. (NCT02562534) | Clinical Trial Compass
TerminatedNot Applicable
Creation of an ECG Database in 3T MRI With Healthy Heart and Several Kind of Cardiac Disease.
Stopped: There was sufficient data to verify the primary endpoint
France19 participantsStarted 2014-01-07
Plain-language summary
The aim is to create a database including recordings of ECG data recorded in an MRI acquisition
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* For all subjects:
* To be more than 18
* To be enroled in a social security plan
* To have signed an informed consent
* To have preliminary medical examination
* For the groups :
* "normal ECG" group : sinus rhythm without conductive troubles. Normal pattern of the QRS
* "conductive troubles group" : patients with typical right bundle branch block, or typical left bundle branch block pattern.
* "rhythm trouble group" : patients with premature atrial beats or premature ventricular beats
Exclusion Criteria:
* Contraindication: implantable devices (cardiac stimulators, defibrillators, cochlear implants, etc.), metallic foreign bodies
* Impossibility to undergo MRI: claustrophobia, morbid obesity.
* Pregnancy or risk of pregnancy.
* Patients under a measure of legal protection
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1This trial was terminated before completing — do you know why it was stopped, and does that affect whether the ECG or MRI data collected so far is still being used in any meaningful way?
2Since this study was focused on recording ECG signals inside a 3T MRI machine rather than testing a treatment, what would participation have actually involved for someone with a cardiac condition, and would it have had any direct benefit to me?
3The trial was measuring ECG signal quality rather than patient health outcomes — does that mean it was more of a data-collection or engineering study, and would you say there's any clinical relevance to my specific heart condition from this kind of research?
4Given that this trial is terminated and listed as 'not applicable' for phase, are there currently active studies or imaging research programs you'd recommend I look into that are actually enrolling patients with my type of heart disease?
5Since this involved MRI scanning for people with cardiac disease, are there any safety considerations I should be aware of when it comes to 3T MRI and my particular heart condition or any devices I might have, like a pacemaker?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.