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The Effects of Carbohydrates in Irritable Bowel Syndrome (FIBS)

Primary Purpose

Irritable Bowel Syndrome With Diarrhea

Status
Recruiting
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Fructan reintroduction
Placebo reintroduction
Sponsored by
Sahlgrenska University Hospital, Sweden
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Irritable Bowel Syndrome With Diarrhea focused on measuring Fructans, FODMAP, carbohydrates

Eligibility Criteria

18 Years - 50 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • IBS according to ROME IV criteria (with diarrhoea)

Exclusion Criteria:

  • Celiac disease or any other gastroenterology disease (such as inflammatory bowel disease, celiac disease, microscopic colitis, diverticulitis, radiation enteritis).
  • Suspected or known strictures, fistulas or physiological/mechanical GI obstruction, history of gastric bezoar.
  • Appendicectomy and cholecystectomy <3 months.
  • Heart-, liver-, neurological-, or current psychiatric disease, diabetes, obesity (BMI>30), other disease or surgery to the abdomen that affected intestinal function.
  • Implantable or portable electro-mechanical medical devices, e.g. pacemakers.
  • Swallowing disorders/dysphagia to food or pills.
  • Allergy or intolerances to foods.
  • Compliance to a special diet (including vegan, vegetarian, gluten-free or low FODMAP diet).
  • Pregnant or breast feeding.
  • Usage of antibiotics within 4 weeks prior to inclusion
  • Usage of alcohol more than 14 units per week.
  • No new pharmacological treatment during the study period.
  • Medications: laxatives, neuromodulators or opioids (morphine, codeine, tramadol…)

Sites / Locations

  • Sahlgrenska University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Fructan powder

Placebo

Arm Description

2 g of fructan powder 3 times per day for 7 days

2g of placebo (maltodextrin) 3 times per day for 7 days.

Outcomes

Primary Outcome Measures

IBS-SSS
change in irritable bowel syndrome severity scoring system (IBS-SSS) between the 2 groups. IBS-SSS is between 0 and 500, with a higher score meaning more severe symptoms.

Secondary Outcome Measures

visceral sensitivity
measured by a rectal barostat, predictor for a better GI response to a low FODMAP diet and predictor of a worse GI response to fructan reintroduction
change in intestinal gas production
measured by a gas sensing capsule (Atmo), between the 2 groups
change in gas production
measured by breath tests (H2 and CH4) between the 2 groups.
change in microbiota
Fecal microbiota analysis using 16S technique between the 2 groups.
Change in metabolomics profiles
Targeted and untargeted metabolomics in urine, blood and stool samples measured by Liquid and gas chromatography-mass spectrometry between the 2 groups.
change in stool form and frequency
Stool diary between the 2 groups.
GSRS-IBS
change in Gastrointestinal symptom rating scale-IBS (GSRS-IBS) between the 2 groups. GSRS-IBS assesses five GI symptom domains: satiety, abdominal pain, diarrhea, constipation and bloating. The five domains are calculated using the mean of two to four items scored with 7-point Likert scales, with higher scores representing more severe symptoms.
HAD
change in Hospital Anxiety and depression scale (HAD) between the 2 groups. HAD assesses the severity of psychological distress, i.e. anxiety and depression. In this 14-item scale, seven items measure anxiety and the other seven measure depression on a 4-point Likert scale (0-3) which provides a score between 0 (absence) and 21 (high level). Scores higher than 10 on each of the subscales is considered to define clinically relevant anxiety and/or depression.
VSI
change in Visceral sensitivity index (VSI) between the 2 groups. VSI is a 15-item validated scale measuring GI symptom-specific anxiety, i.e. the cognitive, affective, and behavioural response to fear of GI sensations, symptoms, and the context in which these occur. The total score ranges between 0 (no GI-specific anxiety) to 75 (severe GI-specific anxiety).
IBSQOL
change in irritable bowel syndrome quality of life (IBSQOL) questionnaire between the 2 groups. IBSQOL is a disease-specific, self-administered questionnaire, with 30 items measuring nine aspects of health-related quality of life during the past four weeks. The nine domains are emotional health, mental health, sleep, energy, physical functioning, food/diet, social role, physical role and sexual relations. Each question has five or six response options. For each subscale, the score is transformed to a 0-100 scale. A higher score represents a better quality of life.
PHQ12
change in patient health questionnaire 12 (PHQ12) between the 2 groups. The PHQ-15 is a somatic symptom subscale derived from the full PHQ. It inquires about 15 somatic symptoms; each individual symptom is coded as 0, 1, or 2, and the total score ranges from 0 to 30, with higher scores representing more severe symptoms.
CSI
change in Central Sensitization Inventory (CSI) between the 2 groups. The responses were graded on a Likert scale from 0 (never) to 4 (always). The total score ranges from 0 to 100. A higher score suggest higher central sensitization syndrome.
IBS-SSS
change in irritable bowel syndrome severity scoring system (IBS-SSS) between the 2 groups.

Full Information

First Posted
March 26, 2021
Last Updated
October 24, 2022
Sponsor
Sahlgrenska University Hospital, Sweden
Collaborators
Atmo Biosciences Pty Ltd, Beneo-Institute
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1. Study Identification

Unique Protocol Identification Number
NCT04830410
Brief Title
The Effects of Carbohydrates in Irritable Bowel Syndrome
Acronym
FIBS
Official Title
The Effects of Fructans in Irritable Bowel Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 30, 2021 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sahlgrenska University Hospital, Sweden
Collaborators
Atmo Biosciences Pty Ltd, Beneo-Institute

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
Food and their components are often reported as gastrointestinal (GI) symptom triggers in patients with IBS. The current interest in dietary management in IBS, has largely focused on the negative effect of poorly absorbed and subsequently fermented carbohydrates (FODMAP - Fermentable Oligo-, Di-, Mono-saccharides And Polyols). These unabsorbed carbohydrates can generate GI symptoms through osmosis, with increased amount of fluid in the gut lumen, and via modification of gut microbiota composition and function (fermentation and production of gas). Studies assessing diets low in FODMAPs have shown promising results in symptom improvement in some IBS patients, but not in all. The low FODMAP diet, as it is used today, is restrictive and difficult for patients to accommodate in their daily life. Moreover, the effect of this diet on microbiota composition and function is not defined, and there are also concerns that restrictive diets may lead to nutritional inadequacy. Fructan is a specific FODMAP which is built of fructose polymers. Examples of foods that contain fructans are wheat, onion, garlic and banana. The daily dietary intake of fructans varies approximately between 3 and 6 grams. Fructans are potential triggers of GI symptoms in IBS however, they are currently also used as prebiotic supplements. A recent systematic review and meta-analysis concluded that low dosages of fructans do not worsen GI symptoms, but they do increase the beneficial bifidobacteria. It remains unclear whether the potential benefits of fructans outweigh the potential harmful effects in patients with IBS. The investigators are aiming to assess the effects of fructans, as well as predictive factors and mechanisms involved, and to compare with placebo in IBS patients. The investigators will assess GI symptom severity, visceral sensitivity, intestinal gas production, gut immunity and microbiota, and metabolites produced in the gut.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome With Diarrhea
Keywords
Fructans, FODMAP, carbohydrates

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
After a low FODMAP diet, patients will have to reintroduce fructan or placebo powder. Patients will be randomized by a web-mail randomization.The powder bags were prepared and named A or B by the firms Beneo, and the participants and the staff involved in the study will be blinded.
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fructan powder
Arm Type
Experimental
Arm Description
2 g of fructan powder 3 times per day for 7 days
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
2g of placebo (maltodextrin) 3 times per day for 7 days.
Intervention Type
Dietary Supplement
Intervention Name(s)
Fructan reintroduction
Intervention Description
Patients will reintroduce fructan powder after 14-day of a low FODMAP diet
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo reintroduction
Intervention Description
Patients will reintroduce placebo powder after 14-day of a low FODMAP diet
Primary Outcome Measure Information:
Title
IBS-SSS
Description
change in irritable bowel syndrome severity scoring system (IBS-SSS) between the 2 groups. IBS-SSS is between 0 and 500, with a higher score meaning more severe symptoms.
Time Frame
before and after the reintroduction (7days +/-3 days)
Secondary Outcome Measure Information:
Title
visceral sensitivity
Description
measured by a rectal barostat, predictor for a better GI response to a low FODMAP diet and predictor of a worse GI response to fructan reintroduction
Time Frame
Baseline
Title
change in intestinal gas production
Description
measured by a gas sensing capsule (Atmo), between the 2 groups
Time Frame
between baseline and after (7days +/-3 days) of reintroduction
Title
change in gas production
Description
measured by breath tests (H2 and CH4) between the 2 groups.
Time Frame
between baseline and after (7days +/-3 days) of reintroduction
Title
change in microbiota
Description
Fecal microbiota analysis using 16S technique between the 2 groups.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
Change in metabolomics profiles
Description
Targeted and untargeted metabolomics in urine, blood and stool samples measured by Liquid and gas chromatography-mass spectrometry between the 2 groups.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
change in stool form and frequency
Description
Stool diary between the 2 groups.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
GSRS-IBS
Description
change in Gastrointestinal symptom rating scale-IBS (GSRS-IBS) between the 2 groups. GSRS-IBS assesses five GI symptom domains: satiety, abdominal pain, diarrhea, constipation and bloating. The five domains are calculated using the mean of two to four items scored with 7-point Likert scales, with higher scores representing more severe symptoms.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
HAD
Description
change in Hospital Anxiety and depression scale (HAD) between the 2 groups. HAD assesses the severity of psychological distress, i.e. anxiety and depression. In this 14-item scale, seven items measure anxiety and the other seven measure depression on a 4-point Likert scale (0-3) which provides a score between 0 (absence) and 21 (high level). Scores higher than 10 on each of the subscales is considered to define clinically relevant anxiety and/or depression.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
VSI
Description
change in Visceral sensitivity index (VSI) between the 2 groups. VSI is a 15-item validated scale measuring GI symptom-specific anxiety, i.e. the cognitive, affective, and behavioural response to fear of GI sensations, symptoms, and the context in which these occur. The total score ranges between 0 (no GI-specific anxiety) to 75 (severe GI-specific anxiety).
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
IBSQOL
Description
change in irritable bowel syndrome quality of life (IBSQOL) questionnaire between the 2 groups. IBSQOL is a disease-specific, self-administered questionnaire, with 30 items measuring nine aspects of health-related quality of life during the past four weeks. The nine domains are emotional health, mental health, sleep, energy, physical functioning, food/diet, social role, physical role and sexual relations. Each question has five or six response options. For each subscale, the score is transformed to a 0-100 scale. A higher score represents a better quality of life.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
PHQ12
Description
change in patient health questionnaire 12 (PHQ12) between the 2 groups. The PHQ-15 is a somatic symptom subscale derived from the full PHQ. It inquires about 15 somatic symptoms; each individual symptom is coded as 0, 1, or 2, and the total score ranges from 0 to 30, with higher scores representing more severe symptoms.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
CSI
Description
change in Central Sensitization Inventory (CSI) between the 2 groups. The responses were graded on a Likert scale from 0 (never) to 4 (always). The total score ranges from 0 to 100. A higher score suggest higher central sensitization syndrome.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)
Title
IBS-SSS
Description
change in irritable bowel syndrome severity scoring system (IBS-SSS) between the 2 groups.
Time Frame
between baseline, after the low FODMAP diet (14 days) and after reintroduction (7+/-3 days)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: IBS according to ROME IV criteria (with diarrhoea) Exclusion Criteria: Celiac disease or any other gastroenterology disease (such as inflammatory bowel disease, celiac disease, microscopic colitis, diverticulitis, radiation enteritis). Suspected or known strictures, fistulas or physiological/mechanical GI obstruction, history of gastric bezoar. Appendicectomy and cholecystectomy <3 months. Heart-, liver-, neurological-, or current psychiatric disease, diabetes, obesity (BMI>30), other disease or surgery to the abdomen that affected intestinal function. Implantable or portable electro-mechanical medical devices, e.g. pacemakers. Swallowing disorders/dysphagia to food or pills. Allergy or intolerances to foods. Compliance to a special diet (including vegan, vegetarian, gluten-free or low FODMAP diet). Pregnant or breast feeding. Usage of antibiotics within 4 weeks prior to inclusion Usage of alcohol more than 14 units per week. No new pharmacological treatment during the study period. Medications: laxatives, neuromodulators or opioids (morphine, codeine, tramadol…)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Magnus Simrén, MD, PhD
Phone
+46313421000
Email
magnus.simren@medicine.gu.se
Facility Information:
Facility Name
Sahlgrenska University Hospital
City
Göteborg
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Magnus Simrén, MD, PhD
Phone
+46313421000
Email
magnus.simren@medicine.gu.se

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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The Effects of Carbohydrates in Irritable Bowel Syndrome

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