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Trial registered on ANZCTR
Registration number
ACTRN12609000651280
Ethics application status
Not yet submitted
Date submitted
29/07/2009
Date registered
3/08/2009
Date last updated
3/08/2009
Type of registration
Retrospectively registered
Titles & IDs
Public title
A Prospective Study to Investigate the Correlation between Wedged Hepatic Venous Pressure and Direct Portal Venous Pressure during formation or revision of Transjugular Intrahepatic Portosystemic Shunt
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Scientific title
In patients undergoing formation or revision of a transjugular intrahepatic portosystemic shunt, does the wedged hepatic vein pressure acurately reflect the direct portal venous pressure?
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Liver Cirrhosis
243396
0
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Portal Hypertension
243397
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Hepatic Vein Wedge Pressure
243398
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Condition category
Condition code
Oral and Gastrointestinal
239705
239705
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Measurement of wedged hepatic vein pressure. This involves wedging a balloon catheter in a hepatic vein branch and measuring the pressure. This is done immediately prior to the formation of the Transjugular Intrahepatic Portosystemic Shunt. When the portal vein is accessed by the shunt, the direct portal vein pressure is measured. This will be compared to the initial hepatic vein wedge pressure measurements for the purpose of teh study. These measurements will add approximately 5 minutes to the scheduled procedure (which takes approximately 40 minutes in total)
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Intervention code [1]
237036
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Diagnosis / Prognosis
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Comparator / control treatment
Uncontrolled
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Degree of correlation between wedged hepatic vein pressure and direct portal pressure. This will be assessed by measuring hepatic vein wedge pressures at multiple sites then measuring the direct portal venous pressure once the transjugular intrahepatic portosystemic shunt has been formed. The average of the wedged hepatic vein pressures will be compared to the direct portal vein pressure.
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Assessment method [1]
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Timepoint [1]
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At time of formation or revision of transjugular intrahepatic portosystemic shunt
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Secondary outcome [1]
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Nil
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Assessment method [1]
257016
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Timepoint [1]
257016
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Nil
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Eligibility
Key inclusion criteria
Age above 18 years
Patient undergoing formation or revision of Transjugular Intrahepatic POrtosystemic Shunt
Able to give informed consent
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Age under 18 years
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Study design
Purpose of the study
Diagnosis
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
All patients scheduled to undergo formation or revision of a Transjugular Intrahepatic Portosystemic Shunt at a single centre will be invited to participate in the study.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
N/A
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
23/07/2009
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
10
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Royal Prince Alfred Hospital
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Address [1]
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Missenden Rd, Camperdown
New South Wales
2050
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Richard Waugh
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Address
Radiology Department
Royal Prince Alfred Hospital
Missenden Rd Camperdown
NSW 2050
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Ines Nikolovski
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Address [1]
236908
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Royal Prince Alfred Hospital
Missenden Rd Camperdown
NSW 2050
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Country [1]
236908
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Australia
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
239543
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Ethics committee address [1]
239543
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Ethics committee country [1]
239543
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Date submitted for ethics approval [1]
239543
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26/08/2009
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Approval date [1]
239543
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Ethics approval number [1]
239543
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Summary
Brief summary
The intent of the study is to determine the accuracy of currently accepted methods of measurement of degree of liver cirrhosis and portal hypertension. This would primarily benefit patients indirectly and may lead to improvement in the techniques used to measure the severity of liver cirrhosis in the future.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
29984
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Country
29984
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Phone
29984
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Fax
29984
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Email
29984
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Contact person for public queries
Name
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Ines Nikolovski
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Address
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Royal Prince Alfred Hospital
Missenden Rd
Camperdown NSW 2050
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Country
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Australia
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Phone
13231
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+61 2 9515 6111
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Fax
13231
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Email
13231
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[email protected]
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Contact person for scientific queries
Name
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Richard Waugh
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Address
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Radiology Department
Royal Prince Alfred Hospital
Missenden Rd
Camperdown, 2050
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Country
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Australia
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Phone
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+61 2 9515 7444
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Fax
4159
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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