The Efficacy of S-adenosyl Methionine (SAMe) Versus Pentoxiphylline in Patients With Non-alcoholic Steatohepatitis With Fibrosis
Primary Purpose
Non-alcoholic Steatohepatitis
Status
Completed
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
S-adenosylmethionine (SAMe)
pentoxiphylline (PTX)
Sponsored by
About this trial
This is an interventional treatment trial for Non-alcoholic Steatohepatitis
Eligibility Criteria
Inclusion Criteria:
- Age 18 to 70 years
- Persistently abnormal ALT >1.2 times upper limit of normal
- Histological evidence of NASH (Non alcoholic Steatohepatitis) on liver biopsy. The minimal criteria for diagnosis of NASH included the presence of lobular inflammation and fibrosis up to stage 3 as per Burnt stating.
Exclusion Criteria:
- Alcohol intake of more than 40gm / week with features suggestive chronic liver disease .
- Other known cause of chronic liver disease like Hepatitis B,C, autoimmune liver disease, Wilson's disease, alpha 1 antitrypsin deficiency and hemochromatosis, primary biliary cirrhosis, PSC (Primary Sclerosis Cholangitis).
- Patient on Medication like estrogens, amiodarone, MTx, tamoxifen, ATT (Antitubercular Treatment)
- Pregnancy or lactation
- Hypersensitivity to methylxanthines (e.g., caffeine, theophylline,)
- Recent retinal/cerebral hemorrhage
- Acute myocardial infarction or severe cardiac arrhythmias.
- Impaired renal function.
Sites / Locations
- Institute of Liver & Biliary Sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
S-adenosylmethionine (SAMe)
pentoxiphylline (PTX)
Arm Description
Outcomes
Primary Outcome Measures
Biochemical improvement in the form of AST/ALT
Improvement in LSM (Liver Stiffness Measurement) & CAP (Controlled Attenuation Parameter)
Secondary Outcome Measures
Metabolic response in form of anthropometry.
metabolic response in form of anthropometry (BMI, waist circumference).
Fasting lipid profiles
Reduction in uric acid levels
Reduction in pro- inflammatory cytokines
Histological outcome in the form of improvement or non- progression in hepatocyte injury and fibrosis.
Full Information
NCT ID
NCT02231333
First Posted
August 30, 2014
Last Updated
October 25, 2019
Sponsor
Institute of Liver and Biliary Sciences, India
1. Study Identification
Unique Protocol Identification Number
NCT02231333
Brief Title
The Efficacy of S-adenosyl Methionine (SAMe) Versus Pentoxiphylline in Patients With Non-alcoholic Steatohepatitis With Fibrosis
Official Title
A Randomized Controlled Trial to Study the Efficacy of S-adenosyl Methionine (SAMe) Versus Pentoxiphylline in Patients With Non-alcoholic Steatohepatitis With Fibrosis.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
July 1, 2013 (Actual)
Primary Completion Date
July 31, 2015 (Actual)
Study Completion Date
July 31, 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute of Liver and Biliary Sciences, India
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Nonalcoholic fatty liver disease is one the most commonly encountered conditions in a daily outpatient Hepatology clinic. Secondly our country is the diabetic capital of the world and so the incidence of NAFLD (Non Alcoholic Fatty Liver Disease) is expected to rise in the future. It is a spectrum of hepatic pathology, ranging from simple steatosis, steatohepatitis, to cirrhosis. Nonalcoholic steatohepatitis (NASH) is a more advanced form of disease where steatosis is accompanied by hepatocyte injury as well as infiltration of inflammatory cells. Approximately 10-20% of patients with NASH may progress to cirrhosis. NASH is felt to be a major etiology of cryptogenic cirrhosis. Around 6230 human studies out of which 49 RCTs have been done till date to define the appropriate treatment of nonalcoholic steatohepatitis. However, still a controversy and no recommended treatment available till date. Recently published PIVENS trial has shown that Vitamin E has proven benefit in NASH. Other trials have also shown that pentoxiphylline has shown benefit in the form of histological improvement and biochemical improvement in the form of liver enzymes. Role of SAMe has been studied in alcoholic liver disease and showed to improve in both biochemical and histological features. However the usefulness of SAMe in NAFLD is not known till now. Hence this study has been designed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-alcoholic Steatohepatitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
122 (Actual)
8. Arms, Groups, and Interventions
Arm Title
S-adenosylmethionine (SAMe)
Arm Type
Experimental
Arm Title
pentoxiphylline (PTX)
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
S-adenosylmethionine (SAMe)
Intervention Type
Drug
Intervention Name(s)
pentoxiphylline (PTX)
Primary Outcome Measure Information:
Title
Biochemical improvement in the form of AST/ALT
Time Frame
1 Years
Title
Improvement in LSM (Liver Stiffness Measurement) & CAP (Controlled Attenuation Parameter)
Time Frame
1 years
Secondary Outcome Measure Information:
Title
Metabolic response in form of anthropometry.
Description
metabolic response in form of anthropometry (BMI, waist circumference).
Time Frame
1 Years
Title
Fasting lipid profiles
Time Frame
1 Years
Title
Reduction in uric acid levels
Time Frame
1 Years
Title
Reduction in pro- inflammatory cytokines
Time Frame
1 Years
Title
Histological outcome in the form of improvement or non- progression in hepatocyte injury and fibrosis.
Time Frame
1 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18 to 70 years
Persistently abnormal ALT >1.2 times upper limit of normal
Histological evidence of NASH (Non alcoholic Steatohepatitis) on liver biopsy. The minimal criteria for diagnosis of NASH included the presence of lobular inflammation and fibrosis up to stage 3 as per Burnt stating.
Exclusion Criteria:
Alcohol intake of more than 40gm / week with features suggestive chronic liver disease .
Other known cause of chronic liver disease like Hepatitis B,C, autoimmune liver disease, Wilson's disease, alpha 1 antitrypsin deficiency and hemochromatosis, primary biliary cirrhosis, PSC (Primary Sclerosis Cholangitis).
Patient on Medication like estrogens, amiodarone, MTx, tamoxifen, ATT (Antitubercular Treatment)
Pregnancy or lactation
Hypersensitivity to methylxanthines (e.g., caffeine, theophylline,)
Recent retinal/cerebral hemorrhage
Acute myocardial infarction or severe cardiac arrhythmias.
Impaired renal function.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dr Devaraja R, MD
Organizational Affiliation
Institute of Liver and Biliary Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Liver & Biliary Sciences
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110070
Country
India
12. IPD Sharing Statement
Learn more about this trial
The Efficacy of S-adenosyl Methionine (SAMe) Versus Pentoxiphylline in Patients With Non-alcoholic Steatohepatitis With Fibrosis
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