search
Back to results

Noradrenalin vs Terlipressin in Hepatorenal Syndrome

Primary Purpose

Hepatorenal Syndrome

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Terlipressin
Noradrenalin
Sponsored by
University of Turin, Italy
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatorenal Syndrome focused on measuring hepatorenal syndrome, ascites, portal hypertension, cirrhosis

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Hepatorenal syndrome Age: 18-75 years Informed written consent Exclusion Criteria: Multinodular hepatocellular carcinoma (more than 3 nodules) Portal vein thrombosis Ongoing bacterial infection Ongoing or recent (less than one week) bleeding Cardio-pulmonary failure Coronary artery disease Peripheral artery disease Arterial hypertension

Sites / Locations

  • San Giovanni Battista Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

2

1

Arm Description

Terlipressin

Noradrenalin

Outcomes

Primary Outcome Measures

Renal function at the beginning and at the end of therapy

Secondary Outcome Measures

Circulatory function

Full Information

First Posted
August 30, 2006
Last Updated
April 9, 2008
Sponsor
University of Turin, Italy
search

1. Study Identification

Unique Protocol Identification Number
NCT00370253
Brief Title
Noradrenalin vs Terlipressin in Hepatorenal Syndrome
Official Title
Noradrenalin vs Terlipressin in Patients With Hepatorenal Syndrome.A Prospective, Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2008
Overall Recruitment Status
Completed
Study Start Date
September 2006 (undefined)
Primary Completion Date
September 2007 (Actual)
Study Completion Date
September 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Turin, Italy

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether noradrenalin is as effective and safe as terlipressin in the treatment of hepatorenal syndrome
Detailed Description
Hepatorenal syndrome (HRS) is a major complication of cirrhosis; it is characterized by functional renal failure and poor prognosis. Arterial dilation is a key pathogenic event of HRS, leading to reduction of the effective blood volume, homeostatic activation of vasoactive systems and renal vasoconstriction with decrease in renal blood flow. The clinical signs of HRS vary depending on the clinical pattern. HRS type 1 is characterized by a rapidly progressive renal failure; HRS type 2 by a moderate and more stable renal failure. HRS type 1 has a very poor short term prognosis, with a median survival of only about 2 weeks; patients with HRS type 2 have a median survival of about 6 months. The management of HRS still constitutes a major challenge. Liver transplantation is the ideal treatment, but it has important inherent drawbacks, such as the organ shortage and the time needed to perform the transplant, that is too long to consent the survival of these patients. The management of HRS has focused on improving renal function, thus extending patients survival and allowing the performance of the liver transplant. In the last years, remarkable results have been obtained using vasoconstrictor drugs. By improving the effective blood volume, vasoconstrictors induce the suppression of homeostatic vasoactive systems and increase renal blood flow and glomerular filtration rate.Among vasoconstrictors, terlipressin, a V1 vasopressin agonist, has currently the best efficacy pedigree. However, it is expensive and is not available in many countries, including North America. More recently, it was suggested that alpha-adrenergic drugs such noradrenalin and midodrine may be also effective in HRS. Noradrenalin would have the potential advantage of wider availability and of lower cost. The current prospective randomized study was undertaken to assess the efficacy and safety of noradrenalin vs terlipressin in patients with HRS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatorenal Syndrome
Keywords
hepatorenal syndrome, ascites, portal hypertension, cirrhosis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
2
Arm Type
Active Comparator
Arm Description
Terlipressin
Arm Title
1
Arm Type
Experimental
Arm Description
Noradrenalin
Intervention Type
Drug
Intervention Name(s)
Terlipressin
Intervention Description
1mg/4 h per day
Intervention Type
Drug
Intervention Name(s)
Noradrenalin
Intervention Description
0,1 mcg/kg/min
Primary Outcome Measure Information:
Title
Renal function at the beginning and at the end of therapy
Time Frame
two weeks
Secondary Outcome Measure Information:
Title
Circulatory function
Time Frame
two weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hepatorenal syndrome Age: 18-75 years Informed written consent Exclusion Criteria: Multinodular hepatocellular carcinoma (more than 3 nodules) Portal vein thrombosis Ongoing bacterial infection Ongoing or recent (less than one week) bleeding Cardio-pulmonary failure Coronary artery disease Peripheral artery disease Arterial hypertension
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mario Rizzetto, MD
Organizational Affiliation
Division of Gastroenterology and Hepatology, San Giovanni Battista Hospital, Turin, Italy
Official's Role
Study Director
Facility Information:
Facility Name
San Giovanni Battista Hospital
City
Turin
ZIP/Postal Code
10126
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
12297842
Citation
Ortega R, Gines P, Uriz J, Cardenas A, Calahorra B, De Las Heras D, Guevara M, Bataller R, Jimenez W, Arroyo V, Rodes J. Terlipressin therapy with and without albumin for patients with hepatorenal syndrome: results of a prospective, nonrandomized study. Hepatology. 2002 Oct;36(4 Pt 1):941-8. doi: 10.1053/jhep.2002.35819.
Results Reference
background
PubMed Identifier
12143045
Citation
Duvoux C, Zanditenas D, Hezode C, Chauvat A, Monin JL, Roudot-Thoraval F, Mallat A, Dhumeaux D. Effects of noradrenalin and albumin in patients with type I hepatorenal syndrome: a pilot study. Hepatology. 2002 Aug;36(2):374-80. doi: 10.1053/jhep.2002.34343.
Results Reference
background
PubMed Identifier
17560680
Citation
Alessandria C, Ottobrelli A, Debernardi-Venon W, Todros L, Cerenzia MT, Martini S, Balzola F, Morgando A, Rizzetto M, Marzano A. Noradrenalin vs terlipressin in patients with hepatorenal syndrome: a prospective, randomized, unblinded, pilot study. J Hepatol. 2007 Oct;47(4):499-505. doi: 10.1016/j.jhep.2007.04.010. Epub 2007 May 24.
Results Reference
derived

Learn more about this trial

Noradrenalin vs Terlipressin in Hepatorenal Syndrome

We'll reach out to this number within 24 hrs