Effect of Metadoxine on Oxidative Stress in Non-alcoholic Hepatic Steatosis
Primary Purpose
NAFLD, Pre-diabetes
Status
Unknown status
Phase
Phase 4
Locations
Mexico
Study Type
Interventional
Intervention
Metadoxine
Sponsored by
About this trial
This is an interventional treatment trial for NAFLD focused on measuring NAFLD, oxidative stress, malondialdehyde
Eligibility Criteria
Inclusion Criteria:
- Male and female
- 18 to 65 years old
- Ultrasonographic diagnosis of NAFLD
- Prediabetes diagnosis
Exclusion Criteria:
- Alcoholism
- Hepatitis C or B Virus Infection
- Pregnancy
- Autoimmune hepatitis
- Metformin or metadoxine allergy
- Parenteral nutrition in the last month
- Weigh loss greater than 10% in the last month
- Taking vitamin supplements in the last month
Sites / Locations
- Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirán"Recruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Metadoxine
Placebo tablet
Arm Description
Metadoxine 500 mg tablets by mouth every 12 hours for 6 months and metformin 500 mg tablets by mouth every 8 hours for 6 months
Placebo tablet (for Metadoxine) by mouth every 12 hours for 6 months and metformin 500 mg tablets by mouth every 8 hours for 6 months
Outcomes
Primary Outcome Measures
Oxidative stress
Malondialdehyde levels
Secondary Outcome Measures
Full Information
NCT ID
NCT02051842
First Posted
January 30, 2014
Last Updated
January 29, 2019
Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
1. Study Identification
Unique Protocol Identification Number
NCT02051842
Brief Title
Effect of Metadoxine on Oxidative Stress in Non-alcoholic Hepatic Steatosis
Official Title
Effect of Metadoxine on Oxidative Stress in Non-alcoholic Fatty Liver Disease Prediabetic Mexican Patients
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 2016 (undefined)
Primary Completion Date
January 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Oxidative stress is produced by imbalance between reactive oxygen species and antioxidant systems. This state is frequently associated with chronic diseases like obesity, insulin resistance, metabolic syndrome and hepatic steatosis. In the liver, the oxidative stress may trigger the progression of fatty liver disease, from triglyceride accumulation to inflammation, cirrhosis and hepatocellular carcinoma. Thus, the attenuation of oxidative stress, could be an important therapeutic target to lessen the severity of the disease. Until now, there is not a medical treatment to cure non-alcoholic fatty liver disease, but therapies aimed at reducing oxidative stress have been proposed. Metadoxine, an ionic complex of pyridoxine-pyrrolidone molecule, acts as a synthetic antioxidant, forming traps that can reduce free radicals; likewise, metadoxine has a proven capacity to reduce fat liver in alcoholic hepatitis. Finally, in fact that alcoholic and non-alcoholic liver diseases share molecular mechanisms in the generation of oxidative stress, the investigators propose metadoxine as a posssible modifier of the oxidative stress in non-alcoholic liver disease, prediabetic patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
NAFLD, Pre-diabetes
Keywords
NAFLD, oxidative stress, malondialdehyde
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Metadoxine
Arm Type
Experimental
Arm Description
Metadoxine 500 mg tablets by mouth every 12 hours for 6 months and metformin 500 mg tablets by mouth every 8 hours for 6 months
Arm Title
Placebo tablet
Arm Type
Placebo Comparator
Arm Description
Placebo tablet (for Metadoxine) by mouth every 12 hours for 6 months and metformin 500 mg tablets by mouth every 8 hours for 6 months
Intervention Type
Drug
Intervention Name(s)
Metadoxine
Other Intervention Name(s)
Metadoxil, Abrixone
Primary Outcome Measure Information:
Title
Oxidative stress
Description
Malondialdehyde levels
Time Frame
Baseline
Other Pre-specified Outcome Measures:
Title
Oxidative stress
Description
Malondialdehyde levels
Time Frame
3 month follow-up
Title
Oxidative stress
Description
Malondialdehyde levels
Time Frame
6 months follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male and female
18 to 65 years old
Ultrasonographic diagnosis of NAFLD
Prediabetes diagnosis
Exclusion Criteria:
Alcoholism
Hepatitis C or B Virus Infection
Pregnancy
Autoimmune hepatitis
Metformin or metadoxine allergy
Parenteral nutrition in the last month
Weigh loss greater than 10% in the last month
Taking vitamin supplements in the last month
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aldo Torre, M.D., M.Sc.
Phone
54870900
Ext
2711
Email
detoal@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aldo Torre, MD MSci
Organizational Affiliation
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirán"
City
Mexico City
ZIP/Postal Code
14000
Country
Mexico
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aldo Torre, M.D, M.Sc.
Phone
54870900
Ext
2711
Email
detoal@yahoo.com
First Name & Middle Initial & Last Name & Degree
Aldo Torre, MD MSci
12. IPD Sharing Statement
Learn more about this trial
Effect of Metadoxine on Oxidative Stress in Non-alcoholic Hepatic Steatosis
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