Impact of a Short-term Treatment With Canagliflozin (Canacardia-HF)
- Sponsor
- Université de Sherbrooke
- Study ID
- NCT03298009
- Status
- Withdrawn
Conditions
- Heart Failure
- Type2 Diabetes
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Canagliflozin 100mg — DRUG2-week intervention
- Placebo oral capsule — DRUG2-week intervention
- PET imaging — RADIATION1 day postprandial metabolic protocol at the end of treatment: CT scan followed by dynamic and pancorporel imaging
Study Details
It is a mechanistic proof-of-concept study to demonstrate how SGLT-2 inhibitors (Canagliflozin) may have a beneficial role on cardiac energetic efficiency. Patients with type 2 diabetes and with HF diagnosed for at least 3 months will be selected. The participants will be randomized to a double-blind, crossover 2-week placebo vs. Cana 100 mg once daily, an interventional trial with a one-month washout period in between. At the term of the two-week placebo and canagliflozin treatment periods (visits 2 and 4), each participant will undergo an identical postprandial metabolic study with positron emission tomography (PET) and stable isotopic tracer methods.
Key Dates
- Start date
- May 1, 2018
- Status verified
- Dec 2024
- Primary completion
- Jun 30, 2018
- Completion
- Jun 30, 2018
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- CROSSOVER
- Primary purpose
- BASIC_SCIENCE
Arms
- Placebo Comparator: Treatment 1placebo oral capsule will be administered once daily, for 2 weeks
- Experimental: Treatment 2Canagliflozine 100mg once daily, for 2 weeks
Primary Outcome Measure
Change to be observed with canagliflozin on myocardial dietary fatty acid uptake [ Time Frame: 3 months ]
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