NAFLD Clinical Trial
— FFLOfficial title:
Fighting the Fatty Liver Pandemic: Developing Effective Protocols & Local Expertise to Deliver & Evaluate Diet/Lifestyle Interventions for Better Liver & Metabolic Health in India
This study aims to build capacity in India by:
1. Developing tailored protocol methodologies for research including technical capability
in imaging (MRI/S protocols & customised software), dietary intervention delivery,
dietary evaluation, and biochemical analyses, using available local resources in Kerala.
2. Training and enhancing imaging skills of clinical radiographers in Kerala for research
studies
3. Training local professionals and researchers in skills necessary to design, deploy and
evaluate diet/lifestyle interventions, including patient engagement, in Kerala.
This study will deliver and evaluate a simple dietary intervention pilot study in the Kerala
region in conjunction with local nutritionists, healthcare professionals and partner
researchers at PHRI (Population Health and Research Institute, Trivandrum, Kerala, India).
Status | Recruiting |
Enrollment | 84 |
Est. completion date | December 31, 2019 |
Est. primary completion date | July 31, 2019 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years and older |
Eligibility |
Inclusion criteria - aged 18 years or over - Male - Able to give informed consent - NAFLD diagnosis showing Fatty/echo-bright liver on ultrasound within past 3 months - Able to attend yoga sessions - Able to undergo MRI - Consumer of at least 300g (uncooked weight) white rice per day (on average) - No allergy to red rice or lentils - Medically suitable for repeated blood sampling Exclusion criteria - Known or suspected cirrhosis on clinical/histological/radiological grounds - Current or recent history of significant alcohol consumption (>14units per week) - Other documented causes of chronic liver disease including: - Hepatitis B or C infection - Drug-induced liver disease - Alcohol-related liver disease - Autoimmune hepatitis - Wilson's disease, Haemachromatosis - Primary biliary cirrhosis, Primary Sclerosing Cholangitis - Currently taking medication that can induce steatosis (corticosteroids, Amiodarone, Tamoxifen, Methotrexate) - Evidence of any other unstable or untreated clinically significant immunological, endocrine, haematological, gastrointestinal, neurological, neoplastic or psychiatric disease - *Female - A number of gender specific confounders (menstrual cycle, age etc) mean that mechanistic studies in small sample sizes are limited to men. The local cohort being used comprises males only. |
Country | Name | City | State |
---|---|---|---|
India | Population Health and Research Institute | Trivandrum | Kerala |
Lead Sponsor | Collaborator |
---|---|
University of Nottingham | Holistic Health and Research Institute, Trivandrum, Kerala, India, Population Health and Research Institute, Trivandrum, Kerala, india |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in liver fat | Measured by MRI, comparing liver fat pre- and post-intervention. | 1 year | |
Secondary | Change in body composition | Measured by body fat % via bioimpedance | 1 year | |
Secondary | Change in body composition | Measured by BMI (kg/m2) | 1 year | |
Secondary | Change in insulin sensitivity | Measured by oral glucose tolerance test (OGTT) | 1 year |
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