EligibleTrials

Prevention of Post-TIPS Hepatic Encephalopathy by Administration of Rifaximin and Lactulose

Recruiting · NCT04073290 · Interventional (participants receive a specific treatment)

View the official record on ClinicalTrials.gov →
Hypertension

Interventions studied

Lactulose 667 milligram/milliliter Oral SolutionPlacebo oral tabletRifaximin 550 milligram Oral Tablet [XIFAXAN]

What this trial is about

Rationale: Hepatic encephalopathy (HE) is a major and common complication in patients with liver cirrhosis. HE can be classified in the extensive range of neurocognitive deterioration as minimal HE (MHE), covert HE (grade I), or overt HE (OHE, grade II-IV). Liver cirrhosis is the most common cause of portal hypertension (PH). Patients who develop complications of PH, like variceal bleeding or refractory ascites, can benefit from a Transjugular Intrahepatic Portosystemic Shunt (TIPS) placement. Unfortunately, post-TIPS HE is a common and often severe complication. Incidence of new onset or worsening of HE after TIPS is approximately 20-45%. Currently there is no strategy to prevent post-TIPS HE.

Who can take part

Age range
18 Years to 80 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Phase 4
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

6 locations listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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