Efficacy of Lactoferrin as an Adjunct Therapy in Patients With Hepatic Encephalopathy
Hepatic Encephalopathy
About this trial
This is an interventional supportive care trial for Hepatic Encephalopathy
Eligibility Criteria
Inclusion Criteria: 18 years and older. Grade I and II hepatic encephalopathy. Exclusion Criteria: Pregnant and breastfeeding women. Grade III and IV hepatic encephalopathy. Individuals confirmed to be allergic to milk protein
Sites / Locations
- National hepatology and tropical medicine research institute
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
No Intervention
Lactoferrin bovine once a day
Lactoferrin bovine twice a day
Control group
15 patients will be subjected to take 100mg of lactoferrin bovine in the form of sachets twice per day for 15 days.
15 patients will be subjected to take 100mg of lactoferrin bovine in the form of sachets once per day for 15 days.
15 patients will be subjected to take only the standard treatment regimen that is applied at the National hepatology and tropical medicine research institute in Egypt.