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

Last updated: October 11, 2014
Sponsor: University of Padova
Overall Status: Terminated

Phase

2/3

Condition

Hepatic Fibrosis

Liver Failure

Liver Disorders

Treatment

N/A

Clinical Study ID

NCT00742339
1264P
  • Ages 18-75
  • All Genders

Study Summary

From 1999, several studies have showed that the use of vasoconstrictors in association with albumin are effective in the treatment of hepatorenal syndrome (HRS). The rationale of the use of vasoconstrictors together with albumin in the treatment of this severe complication of portal hypertension in patients with cirrhosis is to correct the reduction of the effective circulating volume due to the splanchnic arterial vasodilatation.In most of these studies terlipressin, a derivate of vasopressin, has been used as vasoconstrictor as intravenous boluses moving from an initial dose of 0.5-1 mg/4 hr. In some studies midodrine, an alpha-adrenergic agonist, given by mouth has been used as vasoconstrictor at a dose ranging from 2.5 up to 12.5 tid together with octreotide, an inhibitor of the release of glucagon, given subcutaneously at a dose ranging from 10 µg upt to 200 µg tid. To the day, there isn't a study comparing terlipressin + albumin versus midodrine + octreotide + albumin in the treatment of HRS in patients with cirrhosis.Thus, the aim of the study is to compare terlipressin + albumin vs midodrine + octreotide + albumin in the treatment of the HRS in patients with cirrhosis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients with cirrhosis and diagnosis of HRS type 1 or 2,serum creatinine > 2.5 mg/dl

Exclusion

Exclusion Criteria:

  • Diagnosis of HCC with a staging beyond the Milan Criteria di Milano

  • Septic shock (systolic arterial pressure < 90 mmHg

  • Significant heart or respiratory failure

  • Peripheral arteriophaty clinically significant

  • Previous heart stroke or significant alteration of the ECG

Study Design

Total Participants: 49
Study Start date:
May 01, 2005
Estimated Completion Date:
October 31, 2013

Connect with a study center

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

    Padova, 35100
    Italy

    Site Not Available

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