Alexandria University
Alexandria, 21131, Egypt
NCT Number: NCT05430243
The aim of the present study is to investigate the safety, efficacy and cost-effectiveness of empagliflozin, a sodium glucose transporter 2 inhibitor, as an add on therapy to the standard care for refractory ascites in patients with liver cirrhosis
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Notify Me18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Alexandria, 21131, Egypt
Midodrine will be added if the blood pressure less than 100/70 mmHg during the follow up period (start by dose 5 mg three times daily and up titrate the dose according to the blood pressure monitoring to maximum dose 12.5 mg three times daily.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
once daily empagliflozin 10mg+/- diuretics
diuretics as clinically indicated
Time frame: 3 months
Alexandria University
Other
Empagliflozin in the Management of Cirrhosis-related Refractory Ascites: a Randomized Controlled Trial
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