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Mastiha Treatment for Obese With NAFLD Diagnosis (MAST4HEALTH)

Primary Purpose

Non Alcoholic Fatty Liver Disease

Status
Completed
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
Mastiha
Placebo
Sponsored by
Harokopio University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Non Alcoholic Fatty Liver Disease

Eligibility Criteria

18 Years - 67 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Confirmed NAFLD/NASH
  • 18 years < Age < 67 years
  • BMI > 30 kg/ m2

Exclusion Criteria:

  • Hepatotoxic Medication, Concomitant Liver Disease
  • Decompensated Diabetes Mellitus
  • Dysthyroidism, hypopituitarism, Cushing syndrome / disease
  • Alcohol abuse or drug addiction
  • Clinically or biochemically recognized systemic diseases
  • Pregnancy test, lactation
  • Vegan or lacto- and ovo-lacto- vegetarianism
  • Psychiatric or mental disorder
  • Recent loss in body weight or current diet
  • Any use of antioxidant-phytochemical rich supplement, anti-, pre- or pro-biotics within 3 months pre-intervention
  • Changes in drug treatment for e.g. hypertension, diabetes mellitus, 3 months prior or during the 6month intervention
  • Antibiotic treatment during and 2 months prior to screening

Sites / Locations

  • Harokopio University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Mastiha

Placebo

Arm Description

This arm of patients will receive natural Mastiha supplements at a daily dosage of 2.1 g for a 6 month period.

This arm of patients will receive placebo for a 6 month period.

Outcomes

Primary Outcome Measures

LIF score
Improvement in liver histopathology reflected in reduction of the sensitive LIF score

Secondary Outcome Measures

NAFLD/NASH-related laboratory markers
Liver enzymes improvement, inflammation and oxidative stress markers improvement (e.g. IL-6, IL-10, TNF-α, GSH, Gpx), lipid profile improvement, insulin sensitivity improvement pre- and post- intervention in each intervention arm.
Anthropometric characteristics
BMI pre- and post- intervention in each intervention arm.
Genetic profile
Profiles with a comprehensive set of genetic variants to look for markers implicated in response to Mastiha treatment.
Metabolomic profile
Quantification of endogenous metabolites from different compound classes
Metagenomic profile
Association of gut microbes with Mastiha treatment in NAFLD
Epigenetic profile
Identification of the subset of variably methylated regions with low within-individual variability over the six months period of the study to correlate them to treatment.
Effect of Mastiha on different BMI categories
Identification of the effect of Mastiha on different obesity categories: Class I obesity (BMI ≤ 35) and Class II or III obesity (BMI> 35)

Full Information

First Posted
March 9, 2017
Last Updated
April 6, 2022
Sponsor
Harokopio University
Collaborators
University of Novi Sad, National Research Council, Institute of Clinical Physiology, Italy
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1. Study Identification

Unique Protocol Identification Number
NCT03135873
Brief Title
Mastiha Treatment for Obese With NAFLD Diagnosis
Acronym
MAST4HEALTH
Official Title
Mastiha Treatment for Obese With NAFLD Diagnosis
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
March 8, 2017 (Actual)
Primary Completion Date
June 8, 2019 (Actual)
Study Completion Date
June 8, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Harokopio University
Collaborators
University of Novi Sad, National Research Council, Institute of Clinical Physiology, Italy

4. Oversight

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

5. Study Description

Brief Summary
NAFLD/NASH is one of the most common complications of obesity and diabetes mellitus in Western populations affecting approximately 50% of diabetics and 76% of obese patients. Due to the lack of specialized treatment, many new efforts focus on exploring alternative, non-pharmacologic means for managing the disease, including bioactive substances in fruits, vegetables and plants or their products. Mastiha, a natural product of Greece, consists of a great variety of bioactive phytochemical compounds and demonstrates antioxidant, antiinflammatory, antimicrobial and lipid lowering properties. Taking into account the contribution of oxidative stress and inflammation to NAFLD/NASH pathogenesis, the hypothesis that Mastiha could improve disease aspects is investigated. Thus, design of a multicenter (4 centers across Europe), randomized, double-blind, placebo controlled (parallel arm) clinical trial to assess the effect of Mastiha on clinical course of NAFLD/NASH patients has been conducted. The effectiveness of the proposed intervention will be evaluated via clinical and laboratory markers. MAST4HEALTH aims also at exploring gene-diet interactions and at correlating genetic and epigenetic markers with metabolomic and intestinal microbiota profiles pre- and post- intervention. To this end, patients with confirmed NAFLD/NASH will be allocated to either verum or placebo group. Duration of the intervention will be 6 months and the dosage applied will be 2.1 g daily. NAFLD/NASH diagnosis will be confirmed by MS scanning and the sensitive LiverMultiScan technique. Anthropometric, demographic data, body composition, dietary habits, physical activity, family history and smoking status will be assessed pre- and post- intervention. Biochemical profile, oxidative stress and inflammation, as well as epigenetic and metabolomic profiles will be assessed in blood samples, while the metagenome profile will be examined in stools. Both groups will receive counselling to allow for body weight regulation up to 5%. Compliance will be assessed monthly and side effects will be reported.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non Alcoholic Fatty Liver Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Mastiha
Arm Type
Active Comparator
Arm Description
This arm of patients will receive natural Mastiha supplements at a daily dosage of 2.1 g for a 6 month period.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
This arm of patients will receive placebo for a 6 month period.
Intervention Type
Dietary Supplement
Intervention Name(s)
Mastiha
Intervention Description
Mastiha is a natural product of Greece and has a license of manufactures Foods for Particular Nutritional Uses and of National Organization of Medicines (EOF).
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo is designed to have identical characteristics with verum.
Primary Outcome Measure Information:
Title
LIF score
Description
Improvement in liver histopathology reflected in reduction of the sensitive LIF score
Time Frame
6 months
Secondary Outcome Measure Information:
Title
NAFLD/NASH-related laboratory markers
Description
Liver enzymes improvement, inflammation and oxidative stress markers improvement (e.g. IL-6, IL-10, TNF-α, GSH, Gpx), lipid profile improvement, insulin sensitivity improvement pre- and post- intervention in each intervention arm.
Time Frame
6 months
Title
Anthropometric characteristics
Description
BMI pre- and post- intervention in each intervention arm.
Time Frame
6 months
Title
Genetic profile
Description
Profiles with a comprehensive set of genetic variants to look for markers implicated in response to Mastiha treatment.
Time Frame
6 months
Title
Metabolomic profile
Description
Quantification of endogenous metabolites from different compound classes
Time Frame
6 months
Title
Metagenomic profile
Description
Association of gut microbes with Mastiha treatment in NAFLD
Time Frame
6 months
Title
Epigenetic profile
Description
Identification of the subset of variably methylated regions with low within-individual variability over the six months period of the study to correlate them to treatment.
Time Frame
6 months
Title
Effect of Mastiha on different BMI categories
Description
Identification of the effect of Mastiha on different obesity categories: Class I obesity (BMI ≤ 35) and Class II or III obesity (BMI> 35)
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
67 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Confirmed NAFLD/NASH 18 years < Age < 67 years BMI > 30 kg/ m2 Exclusion Criteria: Hepatotoxic Medication, Concomitant Liver Disease Decompensated Diabetes Mellitus Dysthyroidism, hypopituitarism, Cushing syndrome / disease Alcohol abuse or drug addiction Clinically or biochemically recognized systemic diseases Pregnancy test, lactation Vegan or lacto- and ovo-lacto- vegetarianism Psychiatric or mental disorder Recent loss in body weight or current diet Any use of antioxidant-phytochemical rich supplement, anti-, pre- or pro-biotics within 3 months pre-intervention Changes in drug treatment for e.g. hypertension, diabetes mellitus, 3 months prior or during the 6month intervention Antibiotic treatment during and 2 months prior to screening
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
G V DEDOUSIS, PROF.
Organizational Affiliation
Harokopio University
Official's Role
Study Director
Facility Information:
Facility Name
Harokopio University
City
Athens
State/Province
Attica
ZIP/Postal Code
17671
Country
Greece

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
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26471505
Citation
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Results Reference
derived

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Mastiha Treatment for Obese With NAFLD Diagnosis

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