Echocardiographic Assessment of Intrapulmonary Vasodilatation: Agitated Saline Versus Polygeline

Sponsor
Medical University of Vienna (Other)
Overall Status
Unknown status
CT.gov ID
NCT00343122
Collaborator
(none)
100
1

Study Details

Study Description

Brief Summary

The purpose of the study is to evaluate agitated saline versus polygeline for detection of intrapulmonary vasodilatation in patients with cirrhosis.

Condition or Disease Intervention/Treatment Phase
  • Procedure: echocardiography for intrapulmonary vasodilatation

Detailed Description

Intrapulmonary vasodilatation is a frequent finding in patients with cirrhosis. Its diagnosis is established via contrast enhanced echocardiography. One used method is the contrast agent agitated saline and another frequently used method is the contrast agent polygeline. The purpose of this study is to compare these two echocardiographic contrast agents with respect to their ability to detect intrapulmonary vasodilatation.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Defined Population
Time Perspective:
Prospective
Official Title:
Evaluation of Two Methods for the Echocardiographic Assessment of Intrapulmonary Vasodilatation in Patients With Liver Cirrhosis: Agitated Saline Versus Polygelatine
Study Start Date :
Jun 1, 2006

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • age > 18 years

    • presence of liver cirrhosis

    • evaluation for liver transplantation or transjugular intrahepatic portosystemic shunt

    Exclusion Criteria:
    • inadequate echocardiographic image quality

    • allergies to echocardiographic contrast agents

    • pulmonary valve stenosis

    • pulmonary embolism

    • relevant tricuspid regurgitation

    • cardiomyopathy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Intensive Care Unit 13H1, Dep. of Internal Medicine IV, Medical University of Vienna Vienna Austria A-1090

    Sponsors and Collaborators

    • Medical University of Vienna

    Investigators

    • Principal Investigator: Peter Schenk, MD, Intensive Care Unit 13h1, Dep. of Internal Medicine IV, Medical University of Vienna

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00343122
    Other Study ID Numbers:
    • EK 4462005
    First Posted:
    Jun 22, 2006
    Last Update Posted:
    Sep 17, 2007
    Last Verified:
    Sep 1, 2007
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 17, 2007