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Therapeutic And Dietary Effects Of The Sublimated Mare's Milk Supplement In Patients With Non-Alcoholic Steatohepatitis

Primary Purpose

Non-alcoholic Steatohepatitis

Status
Completed
Phase
Not Applicable
Locations
Kazakhstan
Study Type
Interventional
Intervention
Sublimated mare's milk
Ursodeoxycholic Acid
Sponsored by
Medical Centre Hospital of the President's Affairs Administration, Republic of Kazakhstan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non-alcoholic Steatohepatitis focused on measuring Non-alcoholic Steatohepatitis, Mare milk, Immune markers

Eligibility Criteria

16 Years - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with a verified diagnosis of non-alcoholic steatohepatitis;
  • Aged 16 to 60 years;
  • Absence of an allergic reaction to dairy products;
  • Willingness to consent to participate in the study.
  • Consent to adhere to treatment

Exclusion Criteria:

  • Taking antibiotics, cytostatics and steroids during the last 3 months;
  • Taking alcohol hepatotoxic doses (no more than 30 g alcohol per day for men and not more than 20 g for women);
  • History of oncological diseases;
  • Presence of diabetes mellitus, decompensated forms of diseases, intestinal dyspepsia, hypertension (blood pressure 140/90 mm Hg and more at the time of the initial visit to the doctor), tuberculosis;
  • A positive result of screening for antibodies to viral hepatitis B, C and D, as well as HIV
  • Presence of concomitant diseases of the kidneys, liver, cardiovascular, respiratory and other body systems, oncological, mental health and decompensated endocrine diseases, tuberculosis, and HIV infection;
  • Pregnancy and/or lactation;
  • Patient involvement in other clinical trials within the last 3 months;
  • Refusal to participate in the study.

Sites / Locations

  • Medical Centre Hospital of the President's Affairs Administration

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Other

Active Comparator

Arm Label

Dietary supplement only

Dietary supplement and ursodeoxycholic acid therapy

Ursodeoxycholic acid therapy only

Arm Description

Participants will take a sublimated mare milk of 1 sachet 3 times a day during 2 months.

Patients with non-alcoholic steatohepatitis will take ursodeoxycholic acid (2-3 times/day) combined with the mare's milk supplement (1 sachet, 3 times/day) for two months.

Patients with verified diagnosis of non-alcoholic steatohepatitis would be given treatment of ursodeoxycholic acid (2-3 times/day) for a two-month period.

Outcomes

Primary Outcome Measures

Change in liver function indicators
Blood samples will be taken to determine changes in bilirubin, alanine aminotransferase (ALT), aspartate aminotransferase AST, gamma-glutamyl transpeptidase (GGTP), alkaline phosphatase,
Change in degree of steatosis and fibrosis (fibroelastometry method).
Degree of steatosis and fibrosis will evaluated via fibroelastometry method.
Change in degree of steatosis and fibrosis (ultrasound method)
Ultrasound will be used for assessment of steatosis and fibrosis.

Secondary Outcome Measures

Change in biochemical blood test results (cholesterol, glucose)
Proportion of those with deviations from normal range will be reported and compared across periods and groups.
Change in weight.
Frequency of patients with decreased weight will be detected and compared across groups/periods.
Detection of general clinical symptoms of non-alcoholic steatohepatitis.
Symptoms such as of malaise, abdominal discomfort, vague right upper quadrant abdominal pain will be identified in patients during physical examination.

Full Information

First Posted
September 6, 2018
Last Updated
February 3, 2021
Sponsor
Medical Centre Hospital of the President's Affairs Administration, Republic of Kazakhstan
Collaborators
Eurasia Invest Ltd., Ministry of Education and Science, Republic of Kazakhstan
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1. Study Identification

Unique Protocol Identification Number
NCT03664596
Brief Title
Therapeutic And Dietary Effects Of The Sublimated Mare's Milk Supplement In Patients With Non-Alcoholic Steatohepatitis
Official Title
Evaluation Of The Therapeutic And Dietary Properties Of The Sublimated Mare's Milk Supplement In Patients With Non-Alcoholic Steatohepatitis
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
September 1, 2020 (Actual)
Study Completion Date
December 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical Centre Hospital of the President's Affairs Administration, Republic of Kazakhstan
Collaborators
Eurasia Invest Ltd., Ministry of Education and Science, Republic of Kazakhstan

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study evaluates the dietary and therapeutic effect of supplement consisting of sublimated mare milk among patients with non-alcoholic steatohepatitis.
Detailed Description
Nonalcoholic steatohepatitis (NASH) is characterized by the liver damage in the form of fatty degeneration and hepatitis in people who do not abuse alcohol. The disease often develops in middle-aged women with excessive body weight, increased blood glucose and blood lipids, but can occur in all age groups and in both sexes. In most cases, the disease is asymptomatic. Laboratory data indicate an increase in the level of aminotransaminases. Ultrasound reveals hyperechoic tissue of the liver due to diffuse fatty infiltration. The degree of steatosis can also be estimated by a controlled attenuation parameter (CAP - Controlled Attenuation Parameter) in the fibroelastometry of liver tissue. It is also possible to verify the degree of fibrosis of liver tissue in its presence. Given that the mare's milk has therapeutic and dietary properties for various diseases of the internal organs, including liver diseases, the investigators decided to study its therapeutic effectiveness in NASH. In this clinical study, the effectiveness of mare's milk in NASH will be studied in comparison with control groups taking monotherapy with ursodeoxycholic acid (UDCA) and combined therapy (mare's milk and UDCA). Patients will receive a sublimated form of mare's milk in the appropriate dosage within 2 months, and the results of clinical laboratory and instrumental studies will be compared among themselves using statistical methods.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-alcoholic Steatohepatitis
Keywords
Non-alcoholic Steatohepatitis, Mare milk, Immune markers

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
80 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dietary supplement only
Arm Type
Experimental
Arm Description
Participants will take a sublimated mare milk of 1 sachet 3 times a day during 2 months.
Arm Title
Dietary supplement and ursodeoxycholic acid therapy
Arm Type
Other
Arm Description
Patients with non-alcoholic steatohepatitis will take ursodeoxycholic acid (2-3 times/day) combined with the mare's milk supplement (1 sachet, 3 times/day) for two months.
Arm Title
Ursodeoxycholic acid therapy only
Arm Type
Active Comparator
Arm Description
Patients with verified diagnosis of non-alcoholic steatohepatitis would be given treatment of ursodeoxycholic acid (2-3 times/day) for a two-month period.
Intervention Type
Dietary Supplement
Intervention Name(s)
Sublimated mare's milk
Intervention Description
Supplement obtained through sublimation of mare milk, packed into one-dosage sachet (20g), and dissolved in a warm water (36 degrees of Celcius).
Intervention Type
Drug
Intervention Name(s)
Ursodeoxycholic Acid
Intervention Description
Ursodeoxycholic acid in the form of 250 mg capsule.
Primary Outcome Measure Information:
Title
Change in liver function indicators
Description
Blood samples will be taken to determine changes in bilirubin, alanine aminotransferase (ALT), aspartate aminotransferase AST, gamma-glutamyl transpeptidase (GGTP), alkaline phosphatase,
Time Frame
Baseline, Week 2, Week 4, Week 6, Week 8
Title
Change in degree of steatosis and fibrosis (fibroelastometry method).
Description
Degree of steatosis and fibrosis will evaluated via fibroelastometry method.
Time Frame
Baseline, Week 8
Title
Change in degree of steatosis and fibrosis (ultrasound method)
Description
Ultrasound will be used for assessment of steatosis and fibrosis.
Time Frame
Baseline, Week 8
Secondary Outcome Measure Information:
Title
Change in biochemical blood test results (cholesterol, glucose)
Description
Proportion of those with deviations from normal range will be reported and compared across periods and groups.
Time Frame
Baseline, Week 2, Week 4, Week 6, Week 8
Title
Change in weight.
Description
Frequency of patients with decreased weight will be detected and compared across groups/periods.
Time Frame
Baseline, Week 2, Week 4, Week 6, Week 8
Title
Detection of general clinical symptoms of non-alcoholic steatohepatitis.
Description
Symptoms such as of malaise, abdominal discomfort, vague right upper quadrant abdominal pain will be identified in patients during physical examination.
Time Frame
Baseline, Week 2, Week 4, Week 6, Week 8

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with a verified diagnosis of non-alcoholic steatohepatitis; Aged 16 to 60 years; Absence of an allergic reaction to dairy products; Willingness to consent to participate in the study. Consent to adhere to treatment Exclusion Criteria: Taking antibiotics, cytostatics and steroids during the last 3 months; Taking alcohol hepatotoxic doses (no more than 30 g alcohol per day for men and not more than 20 g for women); History of oncological diseases; Presence of diabetes mellitus, decompensated forms of diseases, intestinal dyspepsia, hypertension (blood pressure 140/90 mm Hg and more at the time of the initial visit to the doctor), tuberculosis; A positive result of screening for antibodies to viral hepatitis B, C and D, as well as HIV Presence of concomitant diseases of the kidneys, liver, cardiovascular, respiratory and other body systems, oncological, mental health and decompensated endocrine diseases, tuberculosis, and HIV infection; Pregnancy and/or lactation; Patient involvement in other clinical trials within the last 3 months; Refusal to participate in the study.
Facility Information:
Facility Name
Medical Centre Hospital of the President's Affairs Administration
City
Astana
ZIP/Postal Code
010000
Country
Kazakhstan

12. IPD Sharing Statement

Plan to Share IPD
No
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Therapeutic And Dietary Effects Of The Sublimated Mare's Milk Supplement In Patients With Non-Alcoholic Steatohepatitis

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