Overview

Mechanism and Effects of Manipulating Chloride Homeostasis in Acute Heart Failure

Status:
Recruiting
Trial end date:
2024-03-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to understand the effects of chloride supplementation on volume-overloaded acute heart failure patients concomitantly treated with IV diuretics.
Phase:
Early Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Yale University
Collaborator:
National Heart, Lung, and Blood Institute (NHLBI)
Criteria
Inclusion Criteria:

- Clinical diagnosis of decompensated heart failure with at least one objective sign of
volume overload (rales, edema, elevated jugular venous pressure (JVP), or weight gain
of at least 5 pounds)

- A projected need by the treating clinician for continued treatment with IV diuretics

- Chronic loop diuretic use

Exclusion Criteria:

- Inability to commit to or comply with serial visits for treatment in the Yale
Transitional Care Center (YTCC)

- History of severe metabolic or respiratory acidosis

- Use of metformin, acetazolamide, or any other agent that could predispose to acidosis.
Patients who are on metformin may be enrolled if their metformin can be discontinued
safely for the duration of the study. Any participants who have consistently elevated
Blood glucose readings > 200 mg/dL while inpatient will not be enrolled.

- Serum bicarbonate level <20mmol/L

- Estimated glomerular filtration rate <20 mL/min or renal replacement therapy

- Appears unlikely, or unable to participate in the required study procedures, as
assessed by the study PI or research registered nurse (RN) (ex: clinically-significant
psychiatric, addictive, or neurological disease)

- Inability to give written informed consent or follow study protocol