This trial is seeking to determine whether a single 4mg intranasal dose of bumetanide acutely reduces pulmonary artery pressure and blood volume in the outpatient setting for patients with heart failure and an implanted device for remote patient monitoring (i.e. Cordella or CardioMEMS).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Intranasal route of administration for 4mg of bumetanide
Prisma Health
Greenville, South Carolina, United States
Characterize Temporal Changes
Characterize temporal changes in mean pulmonary artery pressure, systolic pulmonary artery pressure, diastolic pulmonary artery pressure, and heart rate at 1, 2, 3, 6, 12, and 24 hours post-dose of intranasal bumex.
Time frame: 24 hours post-dose
Quantify the Change in Total Blood Volume
Quantify the change in total blood volume in milliliters 24 hours post-dose of intranasal bumex.
Time frame: 24 hours post-dose
Changes in Pertinent Labs
Describe the changes in the following labs at 24 hours post-dose of intranasal bumex: NT-proBNP, serum electrolytes, creatinine, hemoglobin, and hematocrit
Time frame: 24 hours post-dose
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