Effect of Alpha Lipoic Acid on Non-alcoholic Fatty Liver Diseases
Primary Purpose
Non-Alcoholic Fatty Liver Disease
Status
Recruiting
Phase
Phase 4
Locations
India
Study Type
Interventional
Intervention
Placebo
Alphalipoic acid
Sponsored by
About this trial
This is an interventional treatment trial for Non-Alcoholic Fatty Liver Disease focused on measuring Non alcoholic fatty liver, Alphalipoic acid, Nutraceutic, Insulin resistance, Cytokeratin 18, Life style modification, Vitamin E
Eligibility Criteria
Inclusion Criteria:
- All patients diagnosed to have fatty liver grading 1, 2, 3 on abdominal ultrasound, mild to moderate elevation (<5 times elevated upper limit) of serum aminotransferase level.
- Patients aged 18-65 years of either sex.
- Treatment naïve patients or patients who had not taken any treatment for at least 4 weeks before inclusion
Exclusion Criteria:
- History of diabetes mellitus, decompensated liver disease, ascites, oesophageal varices.
- Drug abusers and Alcoholics.
- HBs Ag positive, Anti HCV and HIV, hereditary defects of iron, copper and alpha- 1 antitrypsin deficient patients.
- Hypothyroidism, obstructive sleep apnoea, total parenteral nutrition, short bowel syndrome, pancreatoduodenal resection which are secondary causes of NAFLD.
- Drug users such as corticosteroids, antiviral (nucleoside analogue), tetracycline, methotrexate, tamoxifen and amiodarone.
- Patients who are taking any antihyperlipidemic and anti-diabetic agents.
Sites / Locations
- AIIMSRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
Alphalipoic acid
Arm Description
Life style modification with the placebo will be given for 12 weeks
Life style modification with Alpha lipoic acid in a dose of 600mg twice daily will be prescribed orally for 12 weeks
Outcomes
Primary Outcome Measures
Abdominal ultrasound
the change in fatty liver grading in NAFLD assessed by abdominal ultrasound
Secondary Outcome Measures
Insulin resistance
changes in insulin resistance by using HOMA IR after therapy
Lipid profile
Change in lipid profile (Total Cholesterol, HDL, LDL,Triglycerides, VLDL) after therapy
•
Levels of glutathione reductase
changes in levels of glutathione reductase after therapy
levels of Cytokeratin-18
changes in levels of Cytokeratin-18 after therapy
Levels of Alanine transaminase (ALT)
changes in Alanine transaminase units per litre after therapy
Levels of Aspartate transaminase (AST)
changes in Aspartate transaminase (AST)units per litre after therapy
Levels of Alkaline phosphatase (ALP)
changes in Alkaline phosphatase (ALP) in IU after therapy
Levels of Albumin and total protein.
changes in Albumin and total protein in gm/L after therapy
Levels of Bilirubin
changes in Bilirubin in μmol/L after therapy
Levels of total protein
changes in total protein in gm/L after therapy
Levels of Gamma-glutamyltransferase (GGT).
changes in Gamma-glutamyltransferase (GGT) units per liter after therapy
Levels of L-lactate dehydrogenase (LDH).
changes in L-lactate dehydrogenase (LDH) units per liter after therapy
Full Information
NCT ID
NCT04475276
First Posted
July 10, 2020
Last Updated
July 24, 2023
Sponsor
All India Institute of Medical Sciences, Bhubaneswar
1. Study Identification
Unique Protocol Identification Number
NCT04475276
Brief Title
Effect of Alpha Lipoic Acid on Non-alcoholic Fatty Liver Diseases
Official Title
Effect of Alpha Lipoic Acid on Non-alcoholic Fatty Liver Diseases: A Randomized Placebo-controlled Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 23, 2021 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
November 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
All India Institute of Medical Sciences, Bhubaneswar
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
In developed counties Non-alcoholic fatty liver disease (NAFLD) becomes the most common cause of chronic liver disease , but its prevalence in developing countries like India is also increasing (10 -20%).Till date, there is no US-FDA approved therapy for NAFLD but drugs like metformin, pioglitazone, sitagliptin, vildagliptin Vitamin E, silymarin, statins and ezetimibe have been studied along with life style modification. Life style modifications is the current modality of treatment of NAFLD. All the above-mentioned drugs have some beneficial effects with limited use due to its adverse effects in patients of NAFLD and the study results are non-conclusive. In this scenario, a safe hepatoprotective drug to be evaluated in NAFLD.Alpha-lipoic acid (ALA) or 6,8-thioctic acid, is an endogenous molecule which functions as an important co-factor for various enzyme complexes in mitochondria and plays an important role in energy metabolism. ALA is a nutraceutical agent which also has hepatoprotective and anti-inflammatory effects.ALA is a nutraceutic having anti-inflammatory and antioxidant effects and also increasing insulin sensitivity with lesser adverse effects. The relative scarcity of a promising therapy and non-conclusiveness of the previous studies open up an arena of further research using a nutraceutic in non-diabetic NAFLD. So, the present study is designed to evaluate safety and efficacy of ALA in non-diabetic NAFLD patients.
Detailed Description
In developed counties Non-alcoholic fatty liver disease (NAFLD) becomes the most common cause of chronic liver disease , but its prevalence in developing countries like India is also increasing (10 -20%). Most of the patients are diagnosed clinically and by increased serum transaminase and fatty changes in liver on abdominal ultrasound. Till date, there is no US-FDA approved therapy for NAFLD but drugs like metformin, pioglitazone, sitagliptin, vildagliptin Vitamin E, silymarin, statins and ezetimibe have been studied along with life style modification. Life style modifications is the current modality of treatment of NAFLD. All the above-mentioned drugs have some beneficial effects with limited use due to its adverse effects in patients of NAFLD and the study results are non-conclusive. In this scenario, a safe hepatoprotective drug to be evaluated in NAFLD.
Alpha-lipoic acid (ALA) or 6,8-thioctic acid, is an endogenous molecule which functions as an important co-factor for various enzyme complexes in mitochondria and plays an important role in energy metabolism. ALA is a nutraceutical agent which also has hepatoprotective and anti-inflammatory effects. Previous animal studies proved the hepatoprotective effect of alpha lipoic acid on various animal models. Inflammatory liver injury involves the production of inflammatory mediators like nitric oxide and TNF-alpha. Alpha -Lipoic acid significantly inhibits production of nitric oxide and TNF-alpha. The reduced production of nitric oxide and TNF-alpha in Kupffer cells may be involved in the hepatoprotective action conveyed by alpha-lipoic acid.It has been proved that ALA has potent anti - inflammatory and anti- oxidant properties.
Insulin resistance is associated with impaired hepatic cell damage, intrahepatic cholestasis, atherogenic dyslipidaemia and fibrosis in patients of NAFLD. Daily treatment with ALA for 28 days significantly improved insulin sensitivity performance in mice by decreasing insulin resistance, IL-6 levels, acetylcholinesterase enzyme activity and oxidative stress in liver. Various studies have shown that the ALA can efficiently improve insulin sensitivity and reverse the insulin resistance. Cytokeratin 18 (CK 18) is released into circulation as a consequence of oxidative stress, hepatocyte apoptosis or inflammation in response to lipid metabolism in NAFLD. CK - 18 level is higher in insulin resistance.
ALA is a nutraceutic having anti-inflammatory and antioxidant effects and also increasing insulin sensitivity with lesser adverse effects. The relative scarcity of a promising therapy and non-conclusiveness of the previous studies open up an arena of further research using a nutraceutic in non-diabetic NAFLD. So, the present study is designed to evaluate safety and efficacy of ALA in non-diabetic NAFLD patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Alcoholic Fatty Liver Disease
Keywords
Non alcoholic fatty liver, Alphalipoic acid, Nutraceutic, Insulin resistance, Cytokeratin 18, Life style modification, Vitamin E
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
A randomized, parallel design placebo-controlled clinical trial
Masking
ParticipantCare Provider
Masking Description
The patients and the physician will be blinded
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Life style modification with the placebo will be given for 12 weeks
Arm Title
Alphalipoic acid
Arm Type
Experimental
Arm Description
Life style modification with Alpha lipoic acid in a dose of 600mg twice daily will be prescribed orally for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Lifestyle modification with placebo for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Alphalipoic acid
Intervention Description
Lifestyle modification with Alphalipoic acid for 12 weeks
Primary Outcome Measure Information:
Title
Abdominal ultrasound
Description
the change in fatty liver grading in NAFLD assessed by abdominal ultrasound
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Insulin resistance
Description
changes in insulin resistance by using HOMA IR after therapy
Time Frame
12 weeks
Title
Lipid profile
Description
Change in lipid profile (Total Cholesterol, HDL, LDL,Triglycerides, VLDL) after therapy
•
Time Frame
12 weeks
Title
Levels of glutathione reductase
Description
changes in levels of glutathione reductase after therapy
Time Frame
12 weeks
Title
levels of Cytokeratin-18
Description
changes in levels of Cytokeratin-18 after therapy
Time Frame
12 weeks
Title
Levels of Alanine transaminase (ALT)
Description
changes in Alanine transaminase units per litre after therapy
Time Frame
12 weeks
Title
Levels of Aspartate transaminase (AST)
Description
changes in Aspartate transaminase (AST)units per litre after therapy
Time Frame
12 weeks
Title
Levels of Alkaline phosphatase (ALP)
Description
changes in Alkaline phosphatase (ALP) in IU after therapy
Time Frame
12 weeks
Title
Levels of Albumin and total protein.
Description
changes in Albumin and total protein in gm/L after therapy
Time Frame
12 weeks
Title
Levels of Bilirubin
Description
changes in Bilirubin in μmol/L after therapy
Time Frame
12 weeks
Title
Levels of total protein
Description
changes in total protein in gm/L after therapy
Time Frame
12 weeks
Title
Levels of Gamma-glutamyltransferase (GGT).
Description
changes in Gamma-glutamyltransferase (GGT) units per liter after therapy
Time Frame
12 weeks
Title
Levels of L-lactate dehydrogenase (LDH).
Description
changes in L-lactate dehydrogenase (LDH) units per liter after therapy
Time Frame
12 weeks
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:
All patients diagnosed to have fatty liver grading 1, 2, 3 on abdominal ultrasound, mild to moderate elevation (<5 times elevated upper limit) of serum aminotransferase level.
Patients aged 18-65 years of either sex.
Treatment naïve patients or patients who had not taken any treatment for at least 4 weeks before inclusion
Exclusion Criteria:
History of diabetes mellitus, decompensated liver disease, ascites, oesophageal varices.
Drug abusers and Alcoholics.
HBs Ag positive, Anti HCV and HIV, hereditary defects of iron, copper and alpha- 1 antitrypsin deficient patients.
Hypothyroidism, obstructive sleep apnoea, total parenteral nutrition, short bowel syndrome, pancreatoduodenal resection which are secondary causes of NAFLD.
Drug users such as corticosteroids, antiviral (nucleoside analogue), tetracycline, methotrexate, tamoxifen and amiodarone.
Patients who are taking any antihyperlipidemic and anti-diabetic agents.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Monalisa Jena, MD
Phone
9438884193
Email
drmonalisajena@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rituparna Maiti, MD
Phone
9438884191
Email
pharm_rituparna@aiimsbhubaneswar.edu.in
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rituparna Maiti, MD
Organizational Affiliation
Additional Professor
Official's Role
Study Director
Facility Information:
Facility Name
AIIMS
City
Bhubaneswar
State/Province
Odisha
ZIP/Postal Code
751019
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Monalisa Jena, MD
Phone
9438884193
Email
drmonalisajena@gmail.com
First Name & Middle Initial & Last Name & Degree
Rituparna Maiti, MD
Phone
9438884191
Email
pharm_rituparna@aiimsbhubaneswar.edu.in
12. IPD Sharing Statement
Plan to Share IPD
No
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Effect of Alpha Lipoic Acid on Non-alcoholic Fatty Liver Diseases
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