Clinical Trials · NCT00742339

Terlipressin + Albumin Versus Midodrine + Octreotide in the Treatment of Hepatorenal Syndrome

TerminatedPhase 2/Phase 3Octreotide (Prohibited)
Phase
Phase 2/Phase 3
Recruitment status
Terminated
Sponsor
University of Padova
Enrollment
49
Start date
May 2005
Locations
1 site, Italy
Primary endpoint
The primary end-point of the study is the complete reform of the renal function (serum creatinine < 1.5 mg/dl. The primary end point will be evaluated at the end of the treatment.
View Octreotide compound reference