Trial intelligence / Profile preview

PEG3350 Plus Lactulose vs Lactulose Alone in ACLF With Overt Hepatic Encephalopathy

NCT03987893Phase 4Unknown

Sponsor
Post Graduate Institute of Medical Education and Research
Start
May 2018
Primary completion
May 2020
Modality
Injectable Hydrogels, Implantable Hydrogels, Biodegradable Polymers
Countries
1
01

Overview

Phase 4, randomised, single-blind trial of polyethylene glycol 3350 in hepatic encephalopathy (HE) and acute-on-chronic liver failure (ACLF) (2 arms), sponsored by Post Graduate Institute of Medical Education and Research. Primary endpoints: Improvement in survival at 90 days and Improvement of encephalopathy by one or more grades at 72 hours. Status: unknown.

02

Drugs

polyethylene glycol 3350
03

Conditions

hepatic encephalopathy (HE)acute-on-chronic liver failure (ACLF)

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