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Effect of Pioglitazone on Portal and Systemic Hemodynamics in Patients With Advanced Cirrhosis

Primary Purpose

Cirrhosis, Ascites, Portal Hypertension

Status
Completed
Phase
Phase 4
Locations
Austria
Study Type
Interventional
Intervention
Pioglitazone
Placebo
Sponsored by
Medical University of Vienna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cirrhosis focused on measuring Cirrhosis, oxidative stress, pioglitazone

Eligibility Criteria

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

Inclusion Criteria:

  • Cirrhosis, grade B or C (Child-Pugh score)

Exclusion Criteria:

  • History of hypersensitivity to the trial drugs and contrast agent or to drugs with a similar chemical structure
  • Treatment with vasoactive or non-steroidal anti-inflammatory drugs or systemic antibiotics one week before the study
  • Exclusion criteria for hepatic hemodynamic investigation
  • Cardiac, renal or respiratory failure
  • Previous surgical or transjugular intrahepatic portosystemic shunt
  • Insulin-dependent diabetes

Sites / Locations

  • Internal Medicine III, Gastroenterology and Hepatology, Medical University of Vienna

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

1

2

Arm Description

Patients receive 60mg of pioglitazone once a day orally for 9 days

Patients receive Placebo orally once a day for 9 days

Outcomes

Primary Outcome Measures

portal and systemic hemodynamic parameters

Secondary Outcome Measures

markers of oxidative stress (malondialdehyde)

Full Information

First Posted
December 10, 2007
Last Updated
November 24, 2008
Sponsor
Medical University of Vienna
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1. Study Identification

Unique Protocol Identification Number
NCT00570622
Brief Title
Effect of Pioglitazone on Portal and Systemic Hemodynamics in Patients With Advanced Cirrhosis
Official Title
Effect of Pioglitazone on Portal and Systemic Hemodynamics in Patients With Advanced Cirrhosis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2008
Overall Recruitment Status
Completed
Study Start Date
December 2004 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
November 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Medical University of Vienna

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to investigate the response to pioglitazone on the hepatic venous pressure gradient and peripheral vascular responsiveness to vasoconstrictors in patients with advanced (Child´s Grade B or C) cirrhosis.
Detailed Description
Cirrhotic liver disease is associated with portal hypertension including elevated portal pressure as well as hyperdynamic circulation and low peripheral vascular resistance. Endothelial nitric (NO) release is impaired in liver microvasculature, upregulation of eNOS activity in the cirrhotic liver may constitute a new strategy to correct the increased hepatic vascular tone in these patients. In contrary to this impaired endothelium-dependent relaxation (endothelial dysfunction) and NO deficiency in the cirrhotic liver, systemic and splanchnic circulation of cirrhotic patients is characterized by increased vascular tone and hyporesponsiveness to vasoconstrictors. In addition to increasing insulin sensitivity, thiazolidinediones, like pioglitazone decrease oxidative stress and inflammation and improve endothelial function. In a randomized controlled, parallel group double-blind study 20 Patients with advanced (Child´s Grade B or C) liver cirrhosis will receive pioglitazone or placebo for nine days. Portal hemodynamics and forearm blood flow response will be measured at baseline and after pioglitazone/placebo to investigate the effect of pioglitazone in these group of patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis, Ascites, Portal Hypertension
Keywords
Cirrhosis, oxidative stress, pioglitazone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Patients receive 60mg of pioglitazone once a day orally for 9 days
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Patients receive Placebo orally once a day for 9 days
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Intervention Description
Patients receive 60mg of pioglitazone once a day orally for 9 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Patients receive placebo once a day orally for 9 days
Primary Outcome Measure Information:
Title
portal and systemic hemodynamic parameters
Time Frame
9 days
Secondary Outcome Measure Information:
Title
markers of oxidative stress (malondialdehyde)
Time Frame
9 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cirrhosis, grade B or C (Child-Pugh score) Exclusion Criteria: History of hypersensitivity to the trial drugs and contrast agent or to drugs with a similar chemical structure Treatment with vasoactive or non-steroidal anti-inflammatory drugs or systemic antibiotics one week before the study Exclusion criteria for hepatic hemodynamic investigation Cardiac, renal or respiratory failure Previous surgical or transjugular intrahepatic portosystemic shunt Insulin-dependent diabetes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arnulf Ferlitsch, MD
Organizational Affiliation
Medical University of Vienna
Official's Role
Principal Investigator
Facility Information:
Facility Name
Internal Medicine III, Gastroenterology and Hepatology, Medical University of Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria

12. IPD Sharing Statement

Citations:
PubMed Identifier
16148476
Citation
Ferlitsch A, Pleiner J, Mittermayer F, Schaller G, Homoncik M, Peck-Radosavljevic M, Wolzt M. Vasoconstrictor hyporeactivity can be reversed by antioxidants in patients with advanced alcoholic cirrhosis of the liver and ascites. Crit Care Med. 2005 Sep;33(9):2028-33. doi: 10.1097/01.ccm.0000178173.27923.eb.
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Effect of Pioglitazone on Portal and Systemic Hemodynamics in Patients With Advanced Cirrhosis

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