Impact of Transjugular Intrahepatic Portosystemic Shunts on Liver Stiffness
Stopped early · Not applicable
Conditions studied: Portal Hypertension, Liver Fibroses
In brief
Pilot study examining changes in liver stiffness measured by ultrasound before and after TIPS creation
Key facts
- Study ID
- NCT03352882
- Run by
- University of Pennsylvania
- People needed
- 1
- Starts
- 2016-08-01
- Expected to finish
- 2019-04-03
- Last updated by the study team
- 2019-10-01
Who can join
Age: 18 and older, up to 79. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Symptomatic portal hypertension secondary to cirrhosis undergoing elective outpatient TIPS
- Age >18, Age <80
- Capable of giving informed consent
You may not qualify if…
- Coagulopathy defined as international normalized ration (INR) >2 which cannot be corrected with fresh frozen plasma
- Platelet count <50,000/microliter, which cannot be corrected with platelet transfusion
- BMI >35 and/or cirrhosis due to non-alcoholic steatohepatitis (due to inaccurate elastography measurements in patients with fatty liver)
- Urgent or emergent TIPS for bleeding
- Portal vein thrombosis with in the main, 1st, or 2nd order branches of the portal vein
- Hepatic vein thrombosis (ie no Budd Chiari syndrome)
- Excessive alcohol use defined as more than 2 oz in 24 hours on any individual day within the last 30 days
- Inability to provide informed consent
- Pregnant or nursing women
- Enrollment in concurrent therapeutic trial for symptomatic portal hypertension
Where it is running
- Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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