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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

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?

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000651280
Enrollment
10
Registered
2009-08-03
Start date
2009-07-23
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

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.

Interventions

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

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)

Sponsors

Richard Waugh
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Diagnosis
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Age above 18 years Patient undergoing formation or revision of Transjugular Intrahepatic POrtosystemic Shunt Able to give informed consent

Exclusion criteria

Age under 18 years

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026