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Clinical Trial Summary

The aim of the study is:

- Epidemiological/observational: investigating the presence of neuropsychological and electrophysiological alterations, suggesting a condition of minimal hepatic encephalopathy(and its behavioral correlates), in childhood and young adulthood affected by pre-hepatic portal hypertension due to portal vein thrombosis, even for implementing specific diagnostic protocols.

- Interventional: collecting preliminary data on the effects of a probiotic, in order to implement a controlled clinical study.


Clinical Trial Description

Epidemiological/observational study investigating the presence of neuropsychological and electrophysiological alterations, suggesting a condition of minimal hepatic encephalopathy(and its behavioral correlates), in childhood and young adulthood affected by pre-hepatic portal hypertension due to portal vein thrombosis, even for implementing specific diagnostic protocols ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01798329
Study type Interventional
Source A.O. Ospedale Papa Giovanni XXIII
Contact Lorenzo D'Antiga, MD
Phone +39 0352673856
Email ldantiga@hpg23.it
Status Not yet recruiting
Phase Phase 3
Start date March 2013
Completion date September 2015

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