Spironolactone Versus Spironolactone Plus Furosemide (SVSSF)

PHASE4CompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

April 30, 2005

Primary Completion Date

September 30, 2008

Study Completion Date

September 30, 2008

Conditions
CirrhosisAscites
Interventions
DRUG

Spironolactone and furosemide

Patients in arm A will receive potassium canrenoate at the initial dose of 200 mg/day, then increased up to 400 mg/day. Non responders will be treated with 400 mg/day of potassium canrenoate and furosemide at an initial dose of 50 mg/day, then increased up to 150 mg/day.

DRUG

Spironolactone and furosemide

Patients in arm B will receive at first 200 mg/day of potassium canrenoate and 50 mg/day of furosemide, then increased up to 400 mg/day and 150 mg/day, respectively.

Trial Locations (1)

35100

University of Padova, Dept. of Clinical and Experimental Medicine, Padua

All Listed Sponsors
lead

University of Padova

OTHER

NCT00741663 - Spironolactone Versus Spironolactone Plus Furosemide (SVSSF) | Biotech Hunter | Biotech Hunter