COgnitioN With VERiciGuat Evaluation in Heart Failure
Cognitive Impairment | Heart FailureCONVERGE-HF is a 4-center pilot phase IIb randomized control trial in ambulatory patients with chronic heart failure (≥ 6 months) and mild-to-moderate cognitive impairment.
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Participation Requirements
-
Sex:
ALL -
Eligible Ages:
18 and up
Participation Criteria
Inclusion Criteria:
1. Adult patients
2. Established chronic heart failure (≥ 6 months)
3. Mild-to-moderate cognitive impairment (as per the diagnosis of cognitive impairment or a Montreal Cognitive Assessment (MoCA) score 10-25).
Exclusion Criteria:
1. Patients who have contraindications for sGC stimulator and vericiguat therapy (i.e. use of long-acting nitrates, other soluble guanylate cyclase stimulators (e.g., riociguat), or phosphodiesterase type 5 (PDE-5), pregnancy or breast-feeding)
2. Unable to undergo CMR imaging or brain MRI.
3. CMR exclusions: incompatible implantable cardiac device (ICD or CRT), uncontrolled atrial fibrillation or recurrent ventricular arrhythmias).
4. General medical conditions: uncontrolled thyroid disorders, hepatic failure, or myocardial revascularization procedures \[coronary angioplasty and/or surgical revascularization in the previous 3 months\], cancer/malignancy, or with severe dementia).
5. Patients with allergies to the study products.
6. Patients currently hospitalized.
Study Location
McGill University Health Center
McGill University Health CenterMontreal, Quebec
Canada
Contact Study Team
University of Ottawa
University of OttawaOttawa, Ontario
Canada
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University of Alberta
University of AlbertaEdmonton, Alberta
Canada
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University of Calgary
University of CalgaryCalgary, Alberta
Canada
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- Study Sponsored By
- University of Alberta
- Participants Required
- More Information
- Study ID:
NCT06601465