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Efficacy of Lactoferrin as an Adjunct Therapy in Patients With Hepatic Encephalopathy

Primary Purpose

Hepatic Encephalopathy

Status
Not yet recruiting
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Lactoferrin Bovine
Sponsored by
Al-Azhar University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Hepatic Encephalopathy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Lactoferrin bovine once a day

Lactoferrin bovine twice a day

Control group

Arm Description

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.

Outcomes

Primary Outcome Measures

Change in serum concentration of inflammatory cytokines
Change in serum concentration of inflammatory cytokine Tumor necrosis factor-alpha (TNF-a) (pg/ml)
Change in serum concentration of Nuclear factor kB
Change in serum concentration of Nuclear factor kB (NFkB) (ng/ml)
Change in serum concentration of oxidative stress markers
Change in serum concentration of oxidative stress markers Malondialdehyde (MDA) (n.mol/mg/protein) and Glutathione (GSH) (m.mol/mg/protein)

Secondary Outcome Measures

Change in Psychometric Hepatic Encephalopathy Score (PHES)
Number connection test A (NCT-A) - in this test the numbers have to be joined consecutively in ascending numerical order (1, 2, 3…) as quickly as possible.
Change in Psychometric Hepatic Encephalopathy Score (PHES)
Digit symbol test (DST) - in this test the patient is given a series of double-boxes with a number given in the upper part. The task is to draw a symbol pertinent to this number into the lower part of the boxes. Nine fixed pairs of numbers and symbols are given at the top of the test sheet. Test result is the number of boxes correctly filled within 90 seconds.
Change in Psychometric Hepatic Encephalopathy Score (PHES)
Simplified animal naming test (S-ANT) - in this test patients are asked to name as many animals as possible in one minute. Repeats and errors were excluded from the calculation. The number of named animals after one minute was the definitive score.
Length of hospital stay
Length of hospital stay
The rate of adverse events occurring during the treatment
Number of patients who experienced adverse events such as diarrhea, rash, loss of appetite, fatigue, and constipation.
Number of patients transferred to ICU
Number of patients transferred to ICU

Full Information

First Posted
September 21, 2023
Last Updated
October 14, 2023
Sponsor
Al-Azhar University
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1. Study Identification

Unique Protocol Identification Number
NCT06072521
Brief Title
Efficacy of Lactoferrin as an Adjunct Therapy in Patients With Hepatic Encephalopathy
Official Title
Efficacy of Lactoferrin as an Adjunct Therapy in Patients With Hepatic Encephalopathy
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
September 2024 (Anticipated)
Study Completion Date
October 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Al-Azhar University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to evaluate the efficacy of lactoferrin as an adjunct therapy in improving clinical symptoms and laboratory indices in individuals with hepatic encephalopathy.
Detailed Description
Nonabsorbable disaccharides, such as lactulose or lactitol, decrease the absorption of ammonia and are considered a first-line treatment for hepatic encephalopathy. Antimicrobial therapy also is a part of treatment regimen to alter the gut microbiota to create a more favorable microbiome that results in lower endogenous bacterial production of ammonia and Rifaximin is now the preferred antimicrobial agent for the treatment of hepatic encephalopathy. Many researchers have focused on identifying promising therapeutics and prebiotics in the hope of improving the treatment of hepatic encephalopathy, therefore there is a need to add an adjuvant therapy to decrease oxidative stress and pro-inflammatory cytokines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatic Encephalopathy

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
It is a randomized controlled clinical trial (Pilot study) that will be conducted on hepatic encephalopathy patients who will attend to National Hepatology and Tropical Medicine Research Institute, Cairo, Egypt to receive the treatment regimen in concurrence with the Egyptian guidelines of treatment. Eligible patients will randomly assigned in a 1:1:1 ratio to receive lactoferrin (Pravotin@ sachets) as followings: Group I: Patients receive standard care alone (control group) Group II: Patients receive 100mg lactoferrin orally (one sachet (100 mg), one time a day) plus standard care. Group III: Patients receive 200 mg lactoferrin orally (one sachet (100mg), two times a day) plus standard care. Lactoferrin will be administrated in groups II and III for 15 days. The blood samples of all eligible participants and reported signs and symptoms will be collected after 15 days.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lactoferrin bovine once a day
Arm Type
Active Comparator
Arm Description
15 patients will be subjected to take 100mg of lactoferrin bovine in the form of sachets twice per day for 15 days.
Arm Title
Lactoferrin bovine twice a day
Arm Type
Active Comparator
Arm Description
15 patients will be subjected to take 100mg of lactoferrin bovine in the form of sachets once per day for 15 days.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
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.
Intervention Type
Drug
Intervention Name(s)
Lactoferrin Bovine
Other Intervention Name(s)
Pravotin sachets 100 mg
Intervention Description
Lactoferrin bovine with concentration 100 mg will be given to the patients in test groups in the form of sachets.
Primary Outcome Measure Information:
Title
Change in serum concentration of inflammatory cytokines
Description
Change in serum concentration of inflammatory cytokine Tumor necrosis factor-alpha (TNF-a) (pg/ml)
Time Frame
15 days
Title
Change in serum concentration of Nuclear factor kB
Description
Change in serum concentration of Nuclear factor kB (NFkB) (ng/ml)
Time Frame
15 days
Title
Change in serum concentration of oxidative stress markers
Description
Change in serum concentration of oxidative stress markers Malondialdehyde (MDA) (n.mol/mg/protein) and Glutathione (GSH) (m.mol/mg/protein)
Time Frame
15 days
Secondary Outcome Measure Information:
Title
Change in Psychometric Hepatic Encephalopathy Score (PHES)
Description
Number connection test A (NCT-A) - in this test the numbers have to be joined consecutively in ascending numerical order (1, 2, 3…) as quickly as possible.
Time Frame
15 days
Title
Change in Psychometric Hepatic Encephalopathy Score (PHES)
Description
Digit symbol test (DST) - in this test the patient is given a series of double-boxes with a number given in the upper part. The task is to draw a symbol pertinent to this number into the lower part of the boxes. Nine fixed pairs of numbers and symbols are given at the top of the test sheet. Test result is the number of boxes correctly filled within 90 seconds.
Time Frame
15 days
Title
Change in Psychometric Hepatic Encephalopathy Score (PHES)
Description
Simplified animal naming test (S-ANT) - in this test patients are asked to name as many animals as possible in one minute. Repeats and errors were excluded from the calculation. The number of named animals after one minute was the definitive score.
Time Frame
15 days
Title
Length of hospital stay
Description
Length of hospital stay
Time Frame
15 days
Title
The rate of adverse events occurring during the treatment
Description
Number of patients who experienced adverse events such as diarrhea, rash, loss of appetite, fatigue, and constipation.
Time Frame
15 days
Title
Number of patients transferred to ICU
Description
Number of patients transferred to ICU
Time Frame
15 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kholoud E. Ibrahim, Bachelor
Phone
+20 01066645179
Email
Khloud_elsayed@azhar.edu.eg
First Name & Middle Initial & Last Name or Official Title & Degree
Gellan A. Mohamed, Doctoral
Phone
+20 01062602678
Email
gelan.alaa@azhar.edu.eg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amin M. Abdel Baki, Doctoral
Organizational Affiliation
National hepatology and tropical medicine research institute
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Nayira A. Abdel Baky, Doctoral
Organizational Affiliation
Al-Azhar University
Official's Role
Study Director
Facility Information:
Facility Name
National hepatology and tropical medicine research institute
City
Cairo
Country
Egypt
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amin M. Abdel Baki, Physician
Phone
+02 01014502029
Email
dr_amin114@yahoo.com
First Name & Middle Initial & Last Name & Degree
Amin M. Abdel Baki, Physician
First Name & Middle Initial & Last Name & Degree
Kholoud E. Ibrahim, Pharmacist

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29756596
Citation
Bajaj JS. Hepatic encephalopathy: classification and treatment. J Hepatol. 2018 Apr;68(4):838-839. doi: 10.1016/j.jhep.2017.11.005. No abstract available.
Results Reference
background
PubMed Identifier
26164219
Citation
Patidar KR, Bajaj JS. Covert and Overt Hepatic Encephalopathy: Diagnosis and Management. Clin Gastroenterol Hepatol. 2015 Nov;13(12):2048-61. doi: 10.1016/j.cgh.2015.06.039. Epub 2015 Jul 9.
Results Reference
background
PubMed Identifier
32245524
Citation
Elsaid MI, Rustgi VK. Epidemiology of Hepatic Encephalopathy. Clin Liver Dis. 2020 May;24(2):157-174. doi: 10.1016/j.cld.2020.01.001. Epub 2020 Mar 2.
Results Reference
background

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Efficacy of Lactoferrin as an Adjunct Therapy in Patients With Hepatic Encephalopathy

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