Treatment of Nonalcoholic Fatty Liver Disease With Probiotics and Prebiotics
1 other identifier
interventional
20
1 country
1
Brief Summary
The investigators' aim is to determine whether probiotic and prebiotic treatment plus lifestyle advice is more effective in reducing hepatic fat content than lifestyle advice alone in patients with Nonalcoholic Fatty Liver Disease (NAFLD).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Feb 2009
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2009
CompletedFirst Submitted
Initial submission to the registry
March 25, 2009
CompletedFirst Posted
Study publicly available on registry
March 26, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2012
CompletedFebruary 24, 2014
February 1, 2014
2.9 years
March 25, 2009
February 20, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
The primary endpoint is the reduction in hepatic triglyceride content from baseline to week 24.
24 weeks
Secondary Outcomes (5)
The proportion of patients with normal ALT at week 24 will be determined. Normal ALT is defined according to Prati's cutoffs (≤30 IU/l in men and ≤19 IU/l in women).
24 weeks
The proportion of patients with impaired fasting glucose, diabetes, insulin resistance (estimated by the homeostasis model), hypertension, dyslipidemia and metabolic syndrome will be determined both at baseline and during each visit.
24 weeks
The changes in visceral fat will be determined by magnetic resonance imaging at the same session both at baseline and month 12.
12 months
The changes in liver fibrosis will be determined by transient elastography by Fibroscan both at baseline and month 12.
12 months
The percentage of total sequences of individual microbes will be calculated. In particular, the proportion of Firmicutes and Bacteroidetes will be compared between the two treatment arms.
12 months
Study Arms (2)
Lepicol probiotic & prebiotic formula+simple lifestyle advice
ACTIVE COMPARATORSimple lifestyle advice alone
PLACEBO COMPARATORInterventions
NAFLD patients treated with Lepicol probiotic and prebiotic formula for 24 weeks.
NAFLD patients treated with lifestyle advice.
Eligibility Criteria
You may qualify if:
- Age 18 to 70 years
- Fatty liver identified by imaging studies including ultrasound, computer tomography or magnetic resonance imaging
- Elevated alanine aminotransferase (ALT) according to Prati's criteria (\>30 IU/l in men and \>19 IU/l in women)18
- Written informed consent obtained
You may not qualify if:
- Positive hepatitis B surface antigen, anti-hepatitis C virus antibody, or anti-nuclear antibody titer above 1/160
- Alcohol consumption above 30 g per week in men or 20 g per week in women
- ALT above 10 times the upper limit of normal
- Liver decompensation, as evidenced by bilirubin above 50 µmol/l, platelet count below 100 × 109/l, prothrombin time above 1.3 times the upper limit of normal, albumin below 35 g/l, presence of ascites or varices
- Use of systemic corticosteroids and methotrexate in the last 6 months
- Evidence of hepatocellular carcinoma
- Terminal illness or cancer, unless in complete remission for more than 5 years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Cheng Suen Man Shook Hepatitis Center, Institute of Digestive Disease, The Chinese University of Hong Kong, Prince of Wales Hospital
Hong Kong SAR, China
Related Publications (24)
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PMID: 23396737DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
March 25, 2009
First Posted
March 26, 2009
Study Start
February 1, 2009
Primary Completion
January 1, 2012
Study Completion
January 1, 2012
Last Updated
February 24, 2014
Record last verified: 2014-02