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The Effect of Soluble Fiber to Reduce Post-prandial Glycemic Excursion in Adults With Cystic Fibrosis (SOFI)

Primary Purpose

Cystic Fibrosis-related Diabetes, Cystic Fibrosis

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Soluble fiber supplementation
Placebo (for fiber supplementation)
Sponsored by
Institut de Recherches Cliniques de Montreal
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cystic Fibrosis-related Diabetes focused on measuring Diabetes, Fiber, Supplementation, Soluble fiber, Post-prandial blood glucose, Nutrition

Eligibility Criteria

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

Inclusion Criteria:

  • Diagnosed with CF
  • Aged above 18 years
  • CF-Impaired glucose tolerance, CF-indeterminate glucose tolerance (INDET), de-novo diabetes not requiring immediate treatment and diabetes without pharmacological treatment, based on the oral glucose tolerance test (OGTT) performed within three months of the first visit

Exclusion Criteria:

  • Treated or longstanding CFRD
  • Subjects taking medication or affected by conditions that could interfere with glucose metabolism in the last 6 weeks: hemoptysis, fever, IV antibiotic treatment, pregnancy and oral steroids. If a patient presents any sign of infection confirmed by a trained CF pneumologist, OGTT testing is postponed to the next medical appointment 1 months later.
  • Subjects with severe gastrointestinal disease (Crohn disease, coeliac disease and recent (<1 year) history of intestinal occlusion).
  • Subjects with intestinal obstruction history.
  • Allergy to an ingredient in the menu.
  • Corrector or potentiator prescribed within the last 6 months prior to the first visit.

Sites / Locations

  • Institut de recherches cliniques de Montréal

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

Soluble fiber, dose #1

Soluble fiber, dose #2

Placebo

Arm Description

Soluble fiber supplementation with dose #1 (smaller dose) of psyllium fiber.

Soluble fiber supplementation with dose #2 (bigger dose) of psyllium fiber.

A 250 ml placebo solution of orange-flavored water will be drink at breakfast.

Outcomes

Primary Outcome Measures

Plasma glucose area under the curve

Secondary Outcome Measures

Plasma insulin area under the curve
Incretin hormones
Glucagon-like peptide, gastric inhibitory polypeptide
Side effects of the supplement
It will be measure with gastro-intestinal symptoms visual analog scale. There will be 3 continuous scales for gastrointestinal symptoms and 5 continuous scales to evaluate the satiety. Each scale will measure 100 mm. The score is the distance measured in millimeters from the "no pain" anchor to the participant's mark.
Positive incremental area under the curve for post-prandial glucose and insulin excursions
Mean plasma glucose
Percentage of time with plasma glucose concentration a. >8.0 mmol/L, b. >10.0 mmol/L, c. >11.0 mmol/L, and d. <4.0 mmol/L
Post-meal peak plasma glucose
For the breakfast and lunch

Full Information

First Posted
June 14, 2016
Last Updated
July 16, 2018
Sponsor
Institut de Recherches Cliniques de Montreal
Collaborators
Canadian Cystic Fibrosis Foundation, Université de Montréal
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1. Study Identification

Unique Protocol Identification Number
NCT02810691
Brief Title
The Effect of Soluble Fiber to Reduce Post-prandial Glycemic Excursion in Adults With Cystic Fibrosis
Acronym
SOFI
Official Title
The Effect of Soluble Fiber to Reduce Post-prandial Glycemic Excursion in Adults With Cystic Fibrosis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
July 2016 (undefined)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
April 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institut de Recherches Cliniques de Montreal
Collaborators
Canadian Cystic Fibrosis Foundation, Université de Montréal

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
With improved survival, the clinical spectrum of cystic fibrosis (CF), a complex multi systemic disease, continue to evolve. A major emerging complication is CF related diabetes (CFRD) which is occurring in 40-50% of adults. Patients who develop CFRD are at increase risk of morbidity and mortality and they are also facing an increased medical burden with insulin therapy, the only recommended treatment. Accelerated decline in weight and/or pulmonary function start 2 to 4 years before CFRD onset and this period is characterized by frequent Post-Prandial Glycemic (PPG) excursions. Higher PPG excursions are associated with lower pulmonary function and it predicts future CFRD risk. To the improved nutritional status, lung function and survival of patients, the nutritional approach for patients with CF focuses on high-energy high-fat diet and a pancreatic enzyme supplementation. However, such diet also contributes to increased PPG excursions. Based on the beneficial effects of nutrition therapy to improve PPG in other forms of pre-diabetes and diabetes, extending such benefits to patients with CF is important. The investigators aim to test the feasibility and the effectiveness of a viscous fiber supplement to reduce PPG in adult patients with CF. Using a randomized crossover design, the investigators will study the impact of two doses of a viscous fiber supplement as compared to a placebo.
Detailed Description
With improved survival, the clinical spectrum of cystic fibrosis (CF), a complex multi systemic disease, continue to evolve. A major emerging complication is CF related diabetes (CFRD). CFRD is a major co-morbidity occurring in 20% of adolescents and 40-50% of adults and is mainly due to reduced insulin secretion. Patients who develop CFRD are at increase risk of morbidity and mortality and they are also facing an increased medical burden with insulin therapy, the only recommended treatment. Because accelerated decline in weight and/or pulmonary function start 2 to 4 years before CFRD onset and that this period is characterized by frequent Post-Prandial Glycemic (PPG) excursions, the role of these PPG excursions in clinical deterioration have been investigated. The investigators have shown that higher PPG excursions are associated with lower pulmonary function and others have shown that PPG excursions predicts future CFRD risk. Food overconsumption is discouraged in other forms of diabetes to avoid overweight or obesity, but also to prevent an increase in insulin demand. In contrast, nutritional approach for patients with CF focuses on high-energy high-fat diet to meet increased energy requirements. In combination with an appropriate pancreatic enzyme supplementation, this approach contributes significantly to the improved nutritional status, lung function and survival of patients. However, such diet also contributes to increased PPG excursions. Based on the beneficial effects of nutrition therapy to improve PPG in other forms of pre-diabetes and diabetes, extending such benefits to patients with CF is important. In the context of high CF treatment burden, such approach should however be simple and not inducing weight loss. The investigators aim to test the feasibility and the effectiveness of a viscous fiber supplement to reduce PPG in adult patients with CF. Using a randomized crossover design, the investigators will study the impact of two doses of a viscous fiber supplement as compared to a placebo in controlled conditions, in 22 patients, over 8 hours, at the research center with 2 standardized mixed-meals: breakfast and lunch on PPG excursions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis-related Diabetes, Cystic Fibrosis
Keywords
Diabetes, Fiber, Supplementation, Soluble fiber, Post-prandial blood glucose, Nutrition

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Soluble fiber, dose #1
Arm Type
Active Comparator
Arm Description
Soluble fiber supplementation with dose #1 (smaller dose) of psyllium fiber.
Arm Title
Soluble fiber, dose #2
Arm Type
Active Comparator
Arm Description
Soluble fiber supplementation with dose #2 (bigger dose) of psyllium fiber.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
A 250 ml placebo solution of orange-flavored water will be drink at breakfast.
Intervention Type
Dietary Supplement
Intervention Name(s)
Soluble fiber supplementation
Intervention Description
Two different doses of psyllium powder will be diluted in 250 ml of orange-flavored water and drink in 5 minutes before breakfast.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo (for fiber supplementation)
Intervention Description
Placebo will consist of 250 ml of orange-flavored water to be drink in 5 minutes before breakfast.
Primary Outcome Measure Information:
Title
Plasma glucose area under the curve
Time Frame
3 hours
Secondary Outcome Measure Information:
Title
Plasma insulin area under the curve
Time Frame
3 hours
Title
Incretin hormones
Description
Glucagon-like peptide, gastric inhibitory polypeptide
Time Frame
Each 30 minutes, up to 510 minutes, from 8h30 am to 5h00 pm
Title
Side effects of the supplement
Description
It will be measure with gastro-intestinal symptoms visual analog scale. There will be 3 continuous scales for gastrointestinal symptoms and 5 continuous scales to evaluate the satiety. Each scale will measure 100 mm. The score is the distance measured in millimeters from the "no pain" anchor to the participant's mark.
Time Frame
60, 180, 300, 420 and 540 minutes after the beginning of the test
Title
Positive incremental area under the curve for post-prandial glucose and insulin excursions
Time Frame
3 hours
Title
Mean plasma glucose
Time Frame
9 hours (over study period)
Title
Percentage of time with plasma glucose concentration a. >8.0 mmol/L, b. >10.0 mmol/L, c. >11.0 mmol/L, and d. <4.0 mmol/L
Time Frame
9 hours (over study period)
Title
Post-meal peak plasma glucose
Description
For the breakfast and lunch
Time Frame
3 hours after each meal

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with CF Aged above 18 years CF-Impaired glucose tolerance, CF-indeterminate glucose tolerance (INDET), de-novo diabetes not requiring immediate treatment and diabetes without pharmacological treatment, based on the oral glucose tolerance test (OGTT) performed within three months of the first visit Exclusion Criteria: Treated or longstanding CFRD Subjects taking medication or affected by conditions that could interfere with glucose metabolism in the last 6 weeks: hemoptysis, fever, IV antibiotic treatment, pregnancy and oral steroids. If a patient presents any sign of infection confirmed by a trained CF pneumologist, OGTT testing is postponed to the next medical appointment 1 months later. Subjects with severe gastrointestinal disease (Crohn disease, coeliac disease and recent (<1 year) history of intestinal occlusion). Subjects with intestinal obstruction history. Allergy to an ingredient in the menu. Corrector or potentiator prescribed within the last 6 months prior to the first visit.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rémi Rabasa-Lhoret, MD,PhD
Organizational Affiliation
IRCM
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institut de recherches cliniques de Montréal
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H2W 1R7
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

The Effect of Soluble Fiber to Reduce Post-prandial Glycemic Excursion in Adults With Cystic Fibrosis

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