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Terlipressin in Cirrhotic Patients With Recidivation Ascites Treated With Paracentesis and Albumin (TERAS)

Primary Purpose

Cirrhosis

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Terlipressin
Placebo
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis focused on measuring Refractory ascites, Cirrhosis Terlipressin, Paracentesis

Eligibility Criteria

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

Inclusion Criteria:

  • Patient aged 18 years old and more with cirrhosis and refractory ascites define by the international ascites club.
  • Vital status non engaged in the 2 months

Exclusion Criteria:

  • cardiovascular disease : previous or actual angina pectoralis, myocardial infarction, heart failure, rhythm or conduction disorders, repolarisation abnormality on ECG
  • respiratory disease: previous or actual chronic pulmonary insufficiency, asthma
  • uncontrolled hypertension
  • acute portal vein thrombosis (less then 3 months) or currently treated.
  • chronic renal insufficiency (creatin > 15 mg/L)
  • severe hepatic encephalopathy
  • Alcoholic hepatitis or gastrointestinal bleeding in the last 3 months
  • hepatocellular carcinoma
  • severe illness with life threatening
  • pregnant or breastfeeding women

Sites / Locations

  • CARBONELL Nicolas

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Terlipressin

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Mean number of paracentesis between the 2 groups over a 6 months period

Secondary Outcome Measures

Total ascites retrieval
Number of cirrhosis complications groups
Liver transplantation and deaths
Terlipressin safety
Mean number of days of hospitalization
Delay between inclusion and the first rehospitalisation for ascites retrieval

Full Information

First Posted
September 29, 2009
Last Updated
June 12, 2015
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT00986817
Brief Title
Terlipressin in Cirrhotic Patients With Recidivation Ascites Treated With Paracentesis and Albumin
Acronym
TERAS
Official Title
Efficacy of Terlipressin in Cirrhotic Patients With Recidivation Ascites Treated With Paracentesis and Albumin. A Multi-center Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
November 2009 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
April 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Ascites is a common complication of cirrhosis. Sodium restriction and diuretics are the first step treatment. Refractory ascites (not responding to first step treatment) is treated with repeated large volume paracentesis followed by intra venous albumin expansion. In pilot studies vasoconstrictor agents such as terlipressin have shown beneficial effect on ascites production. Therefore the investigators will study the effect of combined therapy with albumin and terlipressin on recidivation ascites.
Detailed Description
About 30% of cirrhotic patients will develop ascites. Sodium restriction and diuretics are the first step treatment. Total paracentesis is used in patients with cirrhosis and tense ascites. Paracentesis alone was found to induce a decrease in effective arterial blood volume. This circulatory dysfunction may induce inhospital complications such as impaired renal function or hyponatremia and is associated with a significant reduction in long term survival. Intravenous albumin administration after paracentesis has been shown to prevent the post paracentesis decrease in arterial blood volume. Paracentesis also induces arteriolar vasodilation which plays a major role in initiating the decrease in arterial blood volume. Therefore, administration of a vasoconstrictor may decrease paracentesis induced arteriolar vasodilation and prevent the resulting decrease in effective arterial blood volume. Two randomised pilot studies suggest that Terlipressin may be as effective as intravenous albumin in preventing a decrease in effective arterial blood volume in patients with cirrhosis treated by paracentesis for tense ascites. The combined treatment, albumin plus terlipressin, could have additional effect and may improve ascites in such patients. In several studies the combined therapy, albumin plus terlipressin, has shown beneficial effect in cirrhotic patients with hepatorenal syndrome characterized by a sever decrease in arterial blood volume and vasodilation. In these studies, combined therapy was well tolerated.The aim of this study is to compare ascites relapse between two groups of cirrhotic patients with recidivation ascites treated by paracentesis and intravenous albumin perfusion plus terlipressin or placebo. In this double blind randomized multi-center trial, all patients receive albumin perfusion at the dose 8 g/l of removed ascites and Terlipressin (1mg) or placebo, administrated before and at the end of the paracentesis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis
Keywords
Refractory ascites, Cirrhosis Terlipressin, Paracentesis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
82 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Terlipressin
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Terlipressin
Intervention Description
Albumin perfusions at the dose 8 g/l of removed ascites and Terlipressin (1mg), administrated before and at the end of the paracentesis.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
albumin perfusion at the dose 8 g/l of removed ascites and placebo, administrated before and at the end of the paracentesis.
Primary Outcome Measure Information:
Title
Mean number of paracentesis between the 2 groups over a 6 months period
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Total ascites retrieval
Time Frame
6 months
Title
Number of cirrhosis complications groups
Time Frame
6 months
Title
Liver transplantation and deaths
Time Frame
6 months
Title
Terlipressin safety
Time Frame
6 months
Title
Mean number of days of hospitalization
Time Frame
6 months
Title
Delay between inclusion and the first rehospitalisation for ascites retrieval
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient aged 18 years old and more with cirrhosis and refractory ascites define by the international ascites club. Vital status non engaged in the 2 months Exclusion Criteria: cardiovascular disease : previous or actual angina pectoralis, myocardial infarction, heart failure, rhythm or conduction disorders, repolarisation abnormality on ECG respiratory disease: previous or actual chronic pulmonary insufficiency, asthma uncontrolled hypertension acute portal vein thrombosis (less then 3 months) or currently treated. chronic renal insufficiency (creatin > 15 mg/L) severe hepatic encephalopathy Alcoholic hepatitis or gastrointestinal bleeding in the last 3 months hepatocellular carcinoma severe illness with life threatening pregnant or breastfeeding women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicolas Carbonell, MD
Organizational Affiliation
Hôpital Saint Antoine
Official's Role
Principal Investigator
Facility Information:
Facility Name
CARBONELL Nicolas
City
Paris
ZIP/Postal Code
75012
Country
France

12. IPD Sharing Statement

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Terlipressin in Cirrhotic Patients With Recidivation Ascites Treated With Paracentesis and Albumin

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