Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHeinrich-Heine University, Duesseldorf
About this trial
This prospective, single-center post-market-follow-up study aims to fill knowledge gaps by combining advanced cardiac MRI/MRS with systemic mitochondrial assays and exercise testing to characterize the energetic and functional impact of IASD therapy in HFrEF patients.
Eligibility criteria
Qualifiers
Ischemic or non-ischemic cardiomyopathy with LVEF ≤ 40%
Patient is eligible and scheduled to receive the Ventura IASD as per the current IFU.
Symptoms: NYHA Class III
Stability: Chronic heart failure for ≥ 6 months on stable, and at least 3 months on guideline-directed medical therapy (GDMT)
Disqualifiers
Hemodynamics: Resting SBP < 90 or > 160 mmHg
Severe PH (PASP >70 mmHg, PVR > 4 Wood Units)
intracardiac thrombus
Severe RV dysfunction (TAPSE <12 mm or RVFAC ≤25%)
Trial design
Treatments tested in this trial
- cardiac MRI
- Functional Testing
Treatment groups
15 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov