Bumetanide vs. Furosemide in Cirrhosis

Recruiting Phase 3 Interventional Study
Cirrhosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
500 (estimated)
Sponsor
Stacy Johnson · Other
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About This Trial
Patients with cirrhosis are frequently hospitalized due to an acute decompensation of their liver disease including bleeding, jaundice, encephalopathy, and volume overload. Volume overload is associated with increased mortality from acute hypoxic respiratory failure, hemorrhage from esophageal varices, and spontaneous bacterial peritonitis. Clinical practice guidelines describe sodium restriction…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * History of liver cirrhosis * Clinician placed an order for bumetanide or furosemide in electronic health record within 24 hours of presentation to the hospital Exclusion Criteria: * Allergy to bumetanide or furosemide * Contraindication to diuretic administration (e.g. activ…
Contacts

Andrea T White, PhD

8015817818

andrea.white@hsc.utah.edu

CONTACT