About this trial

The goal of this study is to better understand the effects of a sodium-glucose transport protein 2 inhibitor, dapagliflozin, added on to standard of care on heart and lung function and circulating metabolites (substances created when our bodies break down food, drugs, or its own tissues) in patients with chronic kidney disease.

Eligibility criteria

Qualifiers

>18 years of age

eGFR 25-60 ml/min/1,73m2 (eGFR = estimated glomerular filtration rate)

On stable doses of diuretics and/or angiotensin converting enzyme inhibitor or angiotensin receptor blocker

Evidence of subclinical heart failure with preserved ejection fraction at their pre-exercise echocardiogram (defined as meeting 3/5 of the American Society of Echocardiography (ASE) criteria for diastolic dysfunction [septal e'<7 cm/wc, average E/e' ratio>14, left atrial volume index >34 mL/m2, and peak TR velocity >2.8 m/sec] or absolute left ventricular longitudinal strain < 18%, left atrial reservoir strain (LARS) < 25% on 2d speckle tracking echocardiography), lack of augmentation of LVLS or LARS during exercise, or peak VO2 Females: ≤ 18 mL/kg/min, peak VO2 Males: ≤ 20 mL/kg/min on cardiopulmonary exercise testing.

Disqualifiers

presence or history of diabetes

coronary revascularization within the last 6 months

hemodynamically significant valvular disease

significant lung disease requiring home oxygen

Trial design

Treatments tested in this trial

  • Dapagliflozin 10 MG [Farxiga]

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

1
Northwestern University60607, ChicagoIllinois, United States

Sponsors and collaborators

Northwestern University

Lead sponsor

National Institutes of Health (NIH)

Collaborator

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator