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Fecal Microbial Transplantation and Fiber Supplementation in Participants With Obesity and Metabolic Syndrome.

Primary Purpose

Obesity, Metabolic Syndrome

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
FMT
Placebo FMT
Prebiotic Fiber
Cellulose
Sponsored by
University of Alberta
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obesity

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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:

      1. Fasting triglyceride ≥1.7 (TG) mmol/L (with or without taking a statin or fibrate)
      2. HDL cholesterol <1.03 mmol/L in males or <1.29 mmol/L in females (with or without taking a statin or fibrate)
      3. Established diagnosis of hypertension OR SBP ≥130 or DBP ≥85 mmHg (with or without taking at least one antihypertensive agent).

Exclusion Criteria:

  • • Systolic blood pressure ≥180 or diastolic blood pressure ≥110 mmHg at screening.

    • Triglyceride ≥6 mmol/L.
    • Acute infectious or inflammatory condition over the presiding 4 weeks.
    • Current or recent use (Previous 6 months) of insulin for diabetes control.
    • History of oropharyngeal or significant esophageal dysphagia, inflammatory bowel disease, colon cancer, or colonic polyps with high grade dysplasia.
    • History of autoimmune conditions or chronic inflammatory condition, such as rheumatoid arthritis, chronic active hepatitis B or C, HIV, chronic pancreatitis, advanced NASH, or liver cirrhosis.
    • Active malignancy.
    • Active substance abuse or excessive EtOH (defined as >2 X 8oz drinks/d).

Sites / Locations

  • Royal Alexandra Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Other

Experimental

Other

Experimental

Arm Label

Control (Placebo FMT and cellulose)

FMT only (FMT followed by cellulose)

Prebiotic only (Placebo FMT and prebiotic fiber)

FMT + prebiotic fiber

Arm Description

Outcomes

Primary Outcome Measures

insulin sensitivity
The primary endpoint is the change in insulin sensitivity between the time of screening and 6 weeks following treatment.

Secondary Outcome Measures

BMI
weight and height will be combined to report changes in BMI in kg/m^2 between baseline and 6 and 12 weeks
Waist to hip circumferences
Changes in waist to hip circumferences between baseline and 6 and 12 weeks
HbA1C
Changes HbA1C between baseline and 6 and 12 weeks
fasting glucose
Changes fasting glucose between baseline and 6 and 12 weeks
oral glucose tolerance
Changes in oral glucose tolerance between baseline and 6 and 12 weeks
Fasting lipid profile
Changes in Fasting lipid profile between baseline and 6 and 12 weeks
blood pressure
Changes in blood pressure between baseline and 6 and 12 weeks
EuroQol five dimensions questionnaire (EQ-5D™)
Changes in EuroQol five dimensions questionnaire scores to arrive at the participants quality of life between baseline and 6 and 12 weeks
SLIM Hunger and Satiety Questionnaire
The SLIM Hunger and satiety questionnaire scores used to arrive at the participants feelings of hunger and satiety. Changes in reported feelings of Hunger and Satiety between baseline and 6 and 12 weeks
serum levels of leptin, adiponectin, ghrelin, CRP, TNF-α, IL-6, LPS, and LPS-binding protein
Changes in serum levels of leptin, adiponectin, ghrelin, CRP, TNF-α, IL-6, LPS, and LPS-binding protein between baseline and 6 and 12 weeks
fecal microbiota composition
Changes in fecal microbiota composition between baseline and 6 and 12 weeks
stool short chain fatty acid composition
Changes in stool short chain fatty acid composition between baseline and 6 and 12 weeks

Full Information

First Posted
March 12, 2018
Last Updated
December 14, 2021
Sponsor
University of Alberta
Collaborators
W. Garfield Weston Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03477916
Brief Title
Fecal Microbial Transplantation and Fiber Supplementation in Participants With Obesity and Metabolic Syndrome.
Official Title
Fecal Microbial Transplantation and Fiber Supplementation in Participants With Obesity and Metabolic Syndrome.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
April 9, 2018 (Actual)
Primary Completion Date
June 1, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alberta
Collaborators
W. Garfield Weston Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed 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: Changes in Body weight and anthropometric parameters between baseline and week 6. Changes in HbA1C, fasting glucose, glucose tolerance test between baseline and week 6 Changes in fasting lipid profile between baseline and week 6 Changes in blood pressure between baseline and week 6 Quality of life and satiety between baseline and week 6 Changes in serum levels of leptin, adiponectin, ghrelin, CRP, TNF-α, IL-6, LPS, LPS-binding protein and zonulin between baseline and week 6 Changes in stool microbiota composition between baseline and week 6 Changes in stool short chain fatty acid composition between baseline and week 6 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: Fasting triglyceride ≥1.7 mmol/L (with or without taking a statin or fibrate) HDL cholesterol <1.03 mmol/L in males or <1.29 mmol/L in females (with or without taking a statin or fibrate) Known diagnosis of hypertension OR systolic blood pressure ≥130 or diastolic blood pressure ≥85 mmHg (with or without taking at least one antihypertensive agent). Study Product, Dose, Route, Regimen FMT: 50 gm of screened and encapsulated single donor stool (approximately 20-30 capsules) taken by mouth on day 1 of the trial after having fasted overnight and completed a bowel prep with Pico-Salax®. Placebo pills will contain microcrystalline cellulose Soluble corn fiber (PROMITOR®: Tate&Lyle) Women: 4.5 gm of PROMITOR by mouth days 1-3 increased to 9 gm daily from day 4 until trial completion. Men: 5.5 gm of PROMITOR by mouth days 1-3 increased to 11 gm by mouth daily from day 4 until trial completion. Resistant Wheat Starch 4 (Fibersym®: MGP Ingredients): Women: 4.5 gm of powdered RS4 by mouth days 1-3 increased to 9 gm by mouth daily from day 4 until trial completion. Men: 5.5gm of powdered RS4 by mouth days 1-3 increased to 11 gm by mouth daily from day 4 until trial completion. Acacia Gum (Pre-Hydrated Gum Arabic: TIC GUMS): Women: 4.5 gm of powdered acacia gum by mouth days 1-3 increased to 9 gm by mouth daily from day 4 until trial completion. Men: 5.5gm of powdered acacia gum by mouth days 1-3 increased to 11 gr by mouth daily from day 4 until trial completion. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Metabolic Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
68 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control (Placebo FMT and cellulose)
Arm Type
Other
Arm Title
FMT only (FMT followed by cellulose)
Arm Type
Experimental
Arm Title
Prebiotic only (Placebo FMT and prebiotic fiber)
Arm Type
Other
Arm Title
FMT + prebiotic fiber
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
FMT
Intervention Description
fecal microbial transplantation (FMT)
Intervention Type
Biological
Intervention Name(s)
Placebo FMT
Intervention Description
Placebo fecal microbial transplantation (FMT)
Intervention Type
Dietary Supplement
Intervention Name(s)
Prebiotic Fiber
Intervention Description
combined fiber supplement of resistant starch type 4, acacia gum, and soluble corn fiber
Intervention Type
Dietary Supplement
Intervention Name(s)
Cellulose
Intervention Description
Cellulose
Primary Outcome Measure Information:
Title
insulin sensitivity
Description
The primary endpoint is the change in insulin sensitivity between the time of screening and 6 weeks following treatment.
Time Frame
Change between the time of screening and 6 weeks following treatment.
Secondary Outcome Measure Information:
Title
BMI
Description
weight and height will be combined to report changes in BMI in kg/m^2 between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
Waist to hip circumferences
Description
Changes in waist to hip circumferences between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
HbA1C
Description
Changes HbA1C between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
fasting glucose
Description
Changes fasting glucose between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
oral glucose tolerance
Description
Changes in oral glucose tolerance between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
Fasting lipid profile
Description
Changes in Fasting lipid profile between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
blood pressure
Description
Changes in blood pressure between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
EuroQol five dimensions questionnaire (EQ-5D™)
Description
Changes in EuroQol five dimensions questionnaire scores to arrive at the participants quality of life between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
SLIM Hunger and Satiety Questionnaire
Description
The SLIM Hunger and satiety questionnaire scores used to arrive at the participants feelings of hunger and satiety. Changes in reported feelings of Hunger and Satiety between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
serum levels of leptin, adiponectin, ghrelin, CRP, TNF-α, IL-6, LPS, and LPS-binding protein
Description
Changes in serum levels of leptin, adiponectin, ghrelin, CRP, TNF-α, IL-6, LPS, and LPS-binding protein between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
fecal microbiota composition
Description
Changes in fecal microbiota composition between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks
Title
stool short chain fatty acid composition
Description
Changes in stool short chain fatty acid composition between baseline and 6 and 12 weeks
Time Frame
Changes between baseline and 6 and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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: Fasting triglyceride ≥1.7 (TG) mmol/L (with or without taking a statin or fibrate) HDL cholesterol <1.03 mmol/L in males or <1.29 mmol/L in females (with or without taking a statin or fibrate) Established diagnosis of hypertension OR SBP ≥130 or DBP ≥85 mmHg (with or without taking at least one antihypertensive agent). Exclusion Criteria: • Systolic blood pressure ≥180 or diastolic blood pressure ≥110 mmHg at screening. Triglyceride ≥6 mmol/L. Acute infectious or inflammatory condition over the presiding 4 weeks. Current or recent use (Previous 6 months) of insulin for diabetes control. History of oropharyngeal or significant esophageal dysphagia, inflammatory bowel disease, colon cancer, or colonic polyps with high grade dysplasia. History of autoimmune conditions or chronic inflammatory condition, such as rheumatoid arthritis, chronic active hepatitis B or C, HIV, chronic pancreatitis, advanced NASH, or liver cirrhosis. Active malignancy. Active substance abuse or excessive EtOH (defined as >2 X 8oz drinks/d).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karen Madsen, PhD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Alexandra Hospital
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T5H 3V9
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34226737
Citation
Mocanu V, Zhang Z, Deehan EC, Kao DH, Hotte N, Karmali S, Birch DW, Samarasinghe KK, Walter J, Madsen KL. Fecal microbial transplantation and fiber supplementation in patients with severe obesity and metabolic syndrome: a randomized double-blind, placebo-controlled phase 2 trial. Nat Med. 2021 Jul;27(7):1272-1279. doi: 10.1038/s41591-021-01399-2. Epub 2021 Jul 5.
Results Reference
result
Links:
URL
http://cegiir.med.ualberta.ca/KarenMadsen.html
Description
Related Info

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Fecal Microbial Transplantation and Fiber Supplementation in Participants With Obesity and Metabolic Syndrome.

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