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Prebiotics in Newly Diagnosed Type 1 Diabetes

Primary Purpose

Type 1 Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Prebiotic
Placebo
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 1 Diabetes focused on measuring Gut microbiota, Glycemic control, Prebiotic, Oligofructose-enriched inulin, Hypoglycemia

Eligibility Criteria

8 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosed with type 1 diabetes (based on Diabetes Canada 2018 Clinical Practice Guideline diagnostic criteria) in the previous 12 months.
  • Age 8 years and above (as per our pilot trial and able to complete the required tests).

Exclusion Criteria:

  • Regular use of medications or supplements that could affect gut microbiota (examples: antibiotics, probiotic or prebiotic supplements, laxatives) within 3 months prior to enrollment.
  • Previous intestinal surgery.
  • Another chronic medical condition that could affect gut microbiota or intestinal permeability (examples: Crohn's disease, Celiac disease, colitis, irritable bowel syndrome)
  • Presence of active infection, pregnancy or lactation.

Sites / Locations

  • University of CalgaryRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Prebiotic

Placebo

Arm Description

Oligofructose-enriched inulin

Maltodextrin

Outcomes

Primary Outcome Measures

Change in frequency of hypoglycemia
Blood glucose <3.9 mmol/L from continuous glucose monitor data

Secondary Outcome Measures

Change in glycemic control
Glycated hemoglobin (A1C)
Change in stimulated C-peptide
Serum collected during a mixed meal tolerance test
Change in Intestinal permeability
Urinary lactulose/mannitol test
Change in Inflammatory marker IL-6
Serum IL-6
Change in quality of life
Diabetes-specific quality of life survey
Change in dietary intake
24 hour dietary recall (energy intake, fat intake, carbohydrate intake, protein intake, fiber intake)
Change in gut microbiota composition
Fecal microbiota taxonomy
Change in gut microbiota function
Fecal microbiota shotgun sequencing
Change in serum metabolite concentration
Serum LC-Qtof-Mass Spec metabolomics

Full Information

First Posted
July 12, 2021
Last Updated
June 30, 2022
Sponsor
University of Calgary
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1. Study Identification

Unique Protocol Identification Number
NCT04963777
Brief Title
Prebiotics in Newly Diagnosed Type 1 Diabetes
Official Title
Effect of Prebiotic Fibre on Glycemic Control, Gut Microbiota, and Intestinal Permeability in Newly Diagnosed (<12 Months) Type 1 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 29, 2022 (Actual)
Primary Completion Date
September 1, 2025 (Anticipated)
Study Completion Date
September 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary

4. Oversight

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

5. Study Description

Brief Summary
Evidence suggests that prebiotic fibre can correct dysbiosis, reduce intestinal permeability and improve glycemic control. The investigators hypothesize that microbial changes induced by prebiotics contribute to gut and endocrine adaptations that reduce glucose fluctuations, including less hyper- and hypoglycemia in type 1 diabetes (T1D). The primary objective is to compare the change in frequency of hypoglycemia from baseline to 6 months in n=144 newly diagnosed (<12 months) individuals with T1D treated with a 6-month course of prebiotic or placebo as an adjunct to insulin. Secondary objectives will be aimed at understanding the mechanisms by which the prebiotics could affect glycemic control.
Detailed Description
The investigators hypothesize that, as an adjunct to insulin, prebiotic supplementation will reduce the frequency of hypoglycemia and improve glycemic variability that is accompanied by enhanced serum C-peptide levels, a reduction in intestinal permeability and systemic inflammation, and altered gut microbiota. Primary Objective To compare the change in frequency of hypoglycemia from baseline to 6 months in newly diagnosed (<12 months) individuals with T1D treated with a 6-month course of prebiotic or placebo as an adjunct to insulin. Secondary Objectives To determine the change in glycemic variability and glycemic control using Continuous Glucose Monitor (CGM) metrics including: percentage change in Time In-, Below-, and Above-Range (i.e. TIR, TBR, and TAR) and A1C from baseline to 6 months in those treated with prebiotic or placebo. To compare the change in stimulated C-peptide and pro-insulin from baseline to 6 months. To determine the change in IP from baseline to 6 months. To determine the change in serum inflammatory markers (IL-6, IFN-gamma, TNF, C-reactive protein, and IL-10). To examine quality of life (QOL) and fear of hypoglycemia ratings, and adverse reactions (severe hypoglycemia, diabetic ketoacidosis, side effects). To examine prebiotic-induced changes in gut microbiota composition and function (shotgun sequencing) and their metabolic by-products (fecal and serum metabolomics).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 1 Diabetes
Keywords
Gut microbiota, Glycemic control, Prebiotic, Oligofructose-enriched inulin, Hypoglycemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Multi-centre placebo controlled double-blind randomized clinical trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The prebiotic and placebo are both white powders with similar sweet taste and dissolve in water.
Allocation
Randomized
Enrollment
144 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Prebiotic
Arm Type
Experimental
Arm Description
Oligofructose-enriched inulin
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Maltodextrin
Intervention Type
Dietary Supplement
Intervention Name(s)
Prebiotic
Intervention Description
Chicory root derived inulin-type fructan (13.2 kcal/day for ages 8-13 years; 26.4 kcal/day for ages ≥14 years)
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Maltodextrin (isocaloric; 13.2 kcal/day for ages 8-13 years; 26.4 kcal/day for ≥14 years)
Primary Outcome Measure Information:
Title
Change in frequency of hypoglycemia
Description
Blood glucose <3.9 mmol/L from continuous glucose monitor data
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Change in glycemic control
Description
Glycated hemoglobin (A1C)
Time Frame
6 months
Title
Change in stimulated C-peptide
Description
Serum collected during a mixed meal tolerance test
Time Frame
6 months
Title
Change in Intestinal permeability
Description
Urinary lactulose/mannitol test
Time Frame
6 months
Title
Change in Inflammatory marker IL-6
Description
Serum IL-6
Time Frame
6 months
Title
Change in quality of life
Description
Diabetes-specific quality of life survey
Time Frame
6 months
Title
Change in dietary intake
Description
24 hour dietary recall (energy intake, fat intake, carbohydrate intake, protein intake, fiber intake)
Time Frame
6 months
Title
Change in gut microbiota composition
Description
Fecal microbiota taxonomy
Time Frame
6 months
Title
Change in gut microbiota function
Description
Fecal microbiota shotgun sequencing
Time Frame
6 months
Title
Change in serum metabolite concentration
Description
Serum LC-Qtof-Mass Spec metabolomics
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with type 1 diabetes (based on Diabetes Canada 2018 Clinical Practice Guideline diagnostic criteria) in the previous 12 months. Age 8 years and above (as per our pilot trial and able to complete the required tests). Exclusion Criteria: Regular use of medications or supplements that could affect gut microbiota (examples: antibiotics, probiotic or prebiotic supplements, laxatives) within 3 months prior to enrollment. Previous intestinal surgery. Another chronic medical condition that could affect gut microbiota or intestinal permeability (examples: Crohn's disease, Celiac disease, colitis, irritable bowel syndrome) Presence of active infection, pregnancy or lactation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Raylene A Reimer, PhD, RD
Phone
403-220-8218
Email
reimer@ucalgary.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Raylene A Reimer, PhD, RD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 1N4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Raylene A Reimer, PhD, RD
Phone
403-220-8218
Email
reimer@ucalgary.ca

12. IPD Sharing Statement

Plan to Share IPD
No

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Prebiotics in Newly Diagnosed Type 1 Diabetes

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