Mayo Clinic
Rochester, Minnesota, 55905, United States
Location status: Recruiting
Location contact
Claire Raphael, M.B.B.S., Ph.D.
PRINCIPAL_INVESTIGATOR
Diana Albers
CONTACT
NCT Number: NCT07093528
To evaluate the effect of CS reducer implantation in patients with HFPEF and CMD on myocardial ischemia, measured by stress myocardial perfusion using cardiovascular magnetic resonance (CMR)
Interested in participating?
Request Info18 year and older
All sexes
Observational
Rochester, Minnesota, 55905, United States
Location status: Recruiting
Claire Raphael, M.B.B.S., Ph.D.
PRINCIPAL_INVESTIGATOR
Diana Albers
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will consent to undergo a 50-minute non-invasive stress perfusion CMR.
Time frame: Baseline, 6 Months
Endocardial:Epicardial Perfusion Ratio is a measure of myocardial blood flow and will be determined by Cardiovascular magnetic resonance (CMR)
Contact information is provided by the study sponsor or research team.
Mayo Clinic
Other
CMR Substudy of Coronary Sinus Reducer for the Management of Symptomatic Heart Failure With a Preserved Ejection Fraction (HFpEF) Associated With Coronary Microvascular Dysfunction (CMD)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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