Echocardiographic Assessment of Intrapulmonary Vasodilatation: Agitated Saline Versus Polygeline
Evaluation of Two Methods for the Echocardiographic Assessment of Intrapulmonary Vasodilatation in Patients With Liver Cirrhosis: Agitated Saline Versus Polygelatine
1 other identifier
observational
100
1 country
1
Brief Summary
The purpose of the study is to evaluate agitated saline versus polygeline for detection of intrapulmonary vasodilatation in patients with cirrhosis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2006
CompletedFirst Submitted
Initial submission to the registry
June 20, 2006
CompletedFirst Posted
Study publicly available on registry
June 22, 2006
CompletedSeptember 17, 2007
September 1, 2007
June 20, 2006
September 14, 2007
Conditions
Keywords
Interventions
Eligibility Criteria
You may qualify if:
- age \> 18 years
- presence of liver cirrhosis
- evaluation for liver transplantation or transjugular intrahepatic portosystemic shunt
You may not qualify if:
- inadequate echocardiographic image quality
- allergies to echocardiographic contrast agents
- pulmonary valve stenosis
- pulmonary embolism
- relevant tricuspid regurgitation
- cardiomyopathy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Intensive Care Unit 13H1, Dep. of Internal Medicine IV, Medical University of Vienna
Vienna, Vienna, A-1090, Austria
Related Publications (1)
Rodriguez-Roisin R, Krowka MJ, Herve P, Fallon MB; ERS Task Force Pulmonary-Hepatic Vascular Disorders (PHD) Scientific Committee. Pulmonary-Hepatic vascular Disorders (PHD). Eur Respir J. 2004 Nov;24(5):861-80. doi: 10.1183/09031936.04.00010904. No abstract available.
PMID: 15516683BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Peter Schenk, MD
Intensive Care Unit 13h1, Dep. of Internal Medicine IV, Medical University of Vienna
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- DEFINED POPULATION
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
June 20, 2006
First Posted
June 22, 2006
Study Start
June 1, 2006
Last Updated
September 17, 2007
Record last verified: 2007-09