Overview

Terlipressin Given As I.V. Boluses Versus Terlipressin Given As Continuous Intravenous Infusion In Patients With Cirrhosis And Type 1 Hepatorenal Syndrome

Status:
Unknown status
Trial end date:
2015-03-01
Target enrollment:
0
Participant gender:
All
Summary
It is well known that terlipressin and albumin improve renal function in patients with cirrhosis and type 1 HRS. In previous studies terlipressin has been used either as intravenous boluses moving from an initial dose of 0.5-1 mg/4 hr or as continuous intravenous infusion at the initial dose of 2 mg/24 h. Up to now the two schedules of i.v. administration of terlipressin have never been compared. Nevertheless, it has been hypothesized that continuous intravenous infusion assures a more steady profile of effect on portal pressure in patients with cirrhosis. Thus, the aim of the study will be to compare terlipressin given as i.v. bolus vs terlipressin given as continuous intravenous infusion in the treatment of type 1 HRS in patients with cirrhosis.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Padova
Treatments:
Lypressin
Terlipressin
Criteria
Inclusion Criteria:

- Patients with cirrhosis and type 1 HRS

Exclusion Criteria:

- HCC beyond the Milan Criteria,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