drugset / Trial / NCT05013502

Empagliflozin in Diuretic Refractory Ascites

NCT05013502

Phase 1 Completed 14 enrolled Stanford University
NaSingle-groupOpen-labelTreatment

Summary

Ascites is the most frequent complication of liver cirrhosis and results in increased morbidity and mortality but current medical management options are limited. Here, the investigators will conduct an interventional single-arm pilot clinical trial toevaluate the feasibility of empagliflozin in managing diuretic-resistant ascites in patients with decompensated cirrhosis. This single site, open label pilot study will enroll participants with decompensated cirrhosis at a single site. Participants will receive empagliflozin 10mg oral tablets once daily for 12 weeks with monitoring for safety and adverse events.

Timeline

Start
2021-11-15
Primary completion
2023-05-30
Completion
2023-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Empagliflozin Small molecule 10 mg Oral

Indications