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Soluble Fiber Supplement
Inulin for Non-alcoholic Fatty Liver Disease (MILE Trial)
N/A
Waitlist Available
Led By Karen Corbin, PhD
Research Sponsored by AdventHealth Translational Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 28 days
Awards & highlights
MILE Trial Summary
This trial will test whether feeding the gut bacteria soluble fiber will help decrease liver fat in obese individuals.
MILE Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 28 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~28 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Absolute Change in Liver Fat
MILE Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: InulinActive Control1 Intervention
Participants will receive inulin, 10 grams TID for 28 days with titration as follows: 10 grams QD for 3 days, 20 grams BID for 4 days with the remaining 21 days at 10 g TID.
Group II: PlaceboPlacebo Group1 Intervention
Participants will receive powdered maltodextrin to provide equivalent calories and macronutrients without any fiber.
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Who is running the clinical trial?
AdventHealth Translational Research InstituteLead Sponsor
48 Previous Clinical Trials
20,124 Total Patients Enrolled
3 Trials studying Non-alcoholic Fatty Liver Disease
1,302 Patients Enrolled for Non-alcoholic Fatty Liver Disease
Translational Research Institute for Metabolism and Diabetes, FloridaLead Sponsor
40 Previous Clinical Trials
3,540 Total Patients Enrolled
2 Trials studying Non-alcoholic Fatty Liver Disease
1,264 Patients Enrolled for Non-alcoholic Fatty Liver Disease
Karen Corbin, PhDPrincipal InvestigatorStudy Principal Investigator
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