A Study Of CS Reducer For Symptomatic Heart Failure With HFpEF And CMD
Recruiting now
Conditions studied: Heart Failure With Preserved Ejection Fraction, Coronary Microvascular Dysfunction
In brief
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)
Key facts
- Study ID
- NCT07093528
- Run by
- Mayo Clinic
- People needed
- 25
- Starts
- 2025-10-16
- Expected to finish
- 2027-08-01
- Last updated by the study team
- 2026-02-27
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥18
- Enrollment in main CS-reducer HFPEF study IRB# 25-002292
You may not qualify if…
- Metal implants that are not suitable for MRI
- Inability or unwillingness of individual to give written informed consent.
Where it is running
- Mayo Clinic — Rochester, Minnesota, United States (enrolling)
Full record on ClinicalTrials.gov
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