Exercise Cardiovascular Magnetic Resonance In Heart Failure With Preserved Ejection Fraction
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorMayo Clinic
About this trial
The purpose of this study is to internally validate low-field Ex-CMR as a noninvasive tool for diagnosing, phenotyping, and risk stratifying HFpEF in patients with exertional dyspnea.
Eligibility criteria
Qualifiers
Informed consent obtained
HFpEF (cardiologist-adjudicated diagnosis as verified by PI, EF≥50%)
Non-cardiac dyspnea (patients have dyspnea but were found on invasive exercise testing not to have HFpEF).
Healthy volunteers with no history of dyspnea or effort intolerance.
Disqualifiers
Contraindication for low-field CMR, as indicated in MRI safety screening checklist (Research Document #1)
Patient inability or unwillingness to undergo Ex-CMR
Cardiac implants, mechanical or biological valve, causing artifacts that compromise the quality of data
Hospitalization for heart failure in the preceding 30 days.
Trial design
Treatments tested in this trial
- Exercise Cardiovascular Magnetic Resonance
Treatment groups
400 Participants
are divided into 3 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov