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Obesity is increasing in western society at a rapid rate and is associated with metabolic and cardiovascular disease. Although genetics, improper diet, and sedentary lifestyle are known to be factors that can cause obesity, there is a new idea that certain gut microbes may also be involved. Patients who are obese tend to have different kinds of gut microbes compared with lean healthy individuals. Previous studies have shown that changing the gut microbes of obese individuals by doing a fecal transplant (FMT) using gut microbes from a lean individual improves insulin resistance. However, the effects were not maintained. In addition, research has highlighted a necessary role for dietary fiber in the maintenance of microbes required for human health and also that increasing dietary fiber can reduce inflammation that is associated with insulin resistance. This project builds on the findings that gut microbes can be modulated by both FMT and dietary fiber supplementation and will examine if combining these two treatments can increase the effectiveness of these treatments.
The objective of this study is to use fecal microbial transplant to change the gut microbes of obese individuals to those seen in lean individuals and then to use fiber supplements to help maintain the beneficial effects. In this study, overweight individuals who have metabolic syndrome will receive a fecal transplant using a pill form and then consume a variety of fiber supplements for 6 weeks. Effects on metabolic parameters, quality of life, weight, and dietary intake will be followed. Microbial composition will be measured in stool samples.
Full description
Phase: This is a phase II clinical trial.
Methodology: This is an exploratory, four-arm, parallel design, randomized placebo-controlled intervention study.
Study Duration: 12 weeks Study Center(s): This is a single center trial at the University of Alberta
Objectives:The objective of this study is to determine if fecal microbial transplantation (FMT) combined with supplementation with a combined fiber supplement of resistant starch type 4, acacia gum, and soluble corn fiber has a clinically significant effect on metabolic outcomes in obese subjects with metabolic syndrome
Primary Outcome: Changes in insulin sensitivity between the time of screening and 6 weeks following treatment.
Secondary Outcomes:
Number of Subjects: 68
Diagnosis and Main Inclusion Criteria
Primary Diagnosis:
• BMI > 30
Key Inclusion Criteria:
Age 18-64 years at screening
Total body weight fluctuation over the last 6 months <10%
Fasting plasma glucose > 5.6 mmol/L OR HgbA1c ≥6.5% (with or without taking an oral antidiabetic medication)
At least one of the following:
Study Product, Dose, Route, Regimen FMT:
Soluble corn fiber (PROMITOR®: Tate&Lyle)
Resistant Wheat Starch 4 (Fibersym®: MGP Ingredients):
Acacia Gum (Pre-Hydrated Gum Arabic: TIC GUMS):
Duration of administration:
FMT: Single dose of 50gm donor stool or placebo (microcrystalline cellulose) on day 1.
Fiber: Daily administration until completion at week 6
Reference therapy Both FMT and Fiber will be placebo matched as reference therapy.
Statistical Methodology: Study groups with by analyzed by pair-wise comparison with evaluation of means between and across groups using paired or unpaired t-tests for continuous outcomes and chi-squared tests for dichotomous ones. Multivariable predictors of change in relevant outcomes will be identified using appropriately constructed and calibrated linear regression models for continuous outcomes or logistic regression models for dichotomous ones.
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Inclusion criteria
• Age ≥ 18 and < 65 years at the time of screening
BMI > 30
Total body weight fluctuation over the last 6 months less than 10%
Fasting plasma glucose (FPG): 1) > 5.6 mmol/L OR Hemoglobin A1c ≥6.5% (with or without taking an oral antidiabetic medication).
At least one of the following criterion:
Exclusion criteria
• Systolic blood pressure ≥180 or diastolic blood pressure ≥110 mmHg at screening.
Primary purpose
Allocation
Interventional model
Masking
68 participants in 4 patient groups
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Data sourced from clinicaltrials.gov
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