GOS to Reduce Symptom Severity in IBS

Irritable Bowel Syndrome Clinical Trial

— EGIS  

Official title:

A Multi-centre, Randomized, Placebo-Controlled, Efficacy Study of Prebiotic Galacto-oligosaccharides on Gastrointestinal Symptom Severity in Patients With Irritable Bowel Syndrome

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05157061
• Other study ID #: EGIS-01
• Status: Recruiting
• Phase: N/A
• Start date: October 26, 2021
• Est. completion date: April 2024

Study information

• Verified date: May 2023
• Source: Clasado
• Contact: Lucien F. Harthoorn, PhD.
• Phone: +44 (0)118 370 2800
• Email: Lucien.Harthoorn[@]clasado.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

IBS is a highly prevalent bowel disorder, characterized by recurrent abdominal pain during bowel movements or a change in bowel habits. Typically, IBS patients experience constipation, diarrhoea or a mix of constipation and diarrhoea, as well as symptoms of abdominal bloating or distension. The chronic and bothersome nature of IBS symptoms negatively affects the quality of life of many patients. Because there are currently limited medical treatment options for IBS, it is important to study new treatments.

IBS can (in part) be caused by an 'imbalance' of the bacteria residing in the intestinal tract. For instance, there may be a lower proportion of specific bacteria that are generally considered beneficial for a persons health. The consumption of non-digestible food ingredients, such as GOS, may stimulate the growth of these beneficial bacteria. GOS is a type of 'prebiotic', which is known to support health and wellbeing of consumers. By restoring the bacterial balance of the intestinal tract, the symptoms of IBS may be reduced after consumption of GOS.

The health effects of the study product (a specific GOS) used in current study was previously investigated in a small group of patients with IBS. Use of the study product indicated a reduction in the patients' symptoms, improvement in the patients' quality of life, and changes in patients' gut bacteria. It is therefore hypothesized that GOS / a specific GOS may reduce the symptom severity of patients with IBS.

This study further evaluates how GOS may improve symptoms of IBS.

Description:

A Phase III, randomized, double-blind, placebo-controlled, multi-centre, 8-week intervention study, preceded by a 2-week run-in period, to assess the efficacy of GOS on symptom severity in adult patients with IBS. The study population will consist of 210 adult patients diagnosed in the past 36 months with IBS-Diarrhoea (N =70), IBS-Constipation (N = 70), or IBS-Mixed (N =70).

Irritable bowel syndrome (IBS) is a highly prevalent and multifaceted functional bowel disorder characterized by recurrent abdominal pain associated with defecation or a change in bowel habits in the absence of detectable structural and biochemical abnormalities. Disordered bowel habits are typically present, such as constipation, diarrhoea or a mix of constipation and diarrhoea, as are symptoms of abdominal bloating/distension. The chronic and bothersome nature of IBS symptoms negatively affects patients' quality of life and introduces a substantial economic burden on patients and the healthcare system. The gut microbiota composition and function may play a pivotal role in the pathogenesis of IBS, as a reduction in endogenous bifidobacteria, lactobacilli, and Faecalibacterium prausnitzii concentrations, as well as small bowel bacterial overgrowth have been reported in IBS patients, thereby introducing the gut microbiota as a potential target for treatment and symptom relief. Intervention with non-digestible food ingredients, such as galacto-oligosaccharides (GOS), may form a suitable intervention strategy, as these 'prebiotics' are known to modulate the gastrointestinal (GI) microbiota and support health and wellbeing of the host.

The safety and efficacy of GOS has previously been evaluated in patients with IBS, which demonstrated that GOS may reduce IBS symptom severity, improve quality of life, improve stool consistency and defecation frequency and alter gut microbiota composition, in a safe manner.

As there are currently limited suitable medical treatments for IBS, this study will evaluate the efficacy of GOS in reducing symptom severity of patients with IBS

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 210
• Est. completion date: April 2024
• Est. primary completion date: February 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Patients who have been diagnosed with IBS by a medically trained person/Health Care Professional (HCP).

2. IBS diagnosis to be confirmed according to the Rome-IV criteria by a primary or secondary care clinician, including a gastroenterologist, at study entry

3. An IBS Symptom Severity Scale score of =125 points at baseline

4. Male or female between 18 and 64 years of age (age ranges included)

5. Possession of a smartphone

6. Willing and eligible to provide consent and comply with protocol and product intake.

Exclusion Criteria:

1. Unclassifiable IBS (IBS-U) as determined by Investigator

2. Use of products marketed as prebiotics, probiotics or synbiotics within 4 weeks prior to study entry (e.g. Yakult, Actimel, Activia, VSL#3, Kefir).

o Regular cheese or yogurt containing lactic acid bacteria are not an exclusion criterion.

3. Systemic antibiotic or antimycotic treatment within 4 weeks prior to study entry

4. Use of laxatives or antidiarrheal medication within 1 week prior to study entry

5. An unstable antidepressant/antipsychotic treatment regimen within 3 months prior to study entry (i.e. treatment should be stable for at least 3 months prior to study entry).

6. Confirmed lactose intolerance, defined as patients who report response to dietary elimination of lactose/dairy products. Confirmation is patient-reported and not done within the scope of this study.

7. Confirmed food allergy, with reported confirmation based on OFC, IgE, or skin prick test. Confirmation is patient-reported and not done within the scope of this study.

8. Galactosemia (galactose metabolism disorder)

9. Following diets likely to affect study outcomes, including:

o low FODMAP, KETO/high-fat, gluten free/coeliac, paleo, weight loss, caloric restriction, low-carb, 5:2/whole day energy restriction, Atkins/high-protein, sugar-free, single-food, juicing/any day of juicing, any other restriction diet (e.g. very low calory), or vegan diets (GOS is derived from cow's milk).

10. Severe illness(es) or medical condition(s), including gastrointestinal pathologies:

o GI ulcers, coeliac disease, inflammatory bowel disease, bowel cancer, bowel resection, , bariatric surgery, acute or chronic diarrhoea secondary to confirmed infectious gastroenteritis, or enteral or parenteral nutrition.

11. Subjects suffering from auto-immune disorders (e.g. Rheumatoid Arthritis, Systemic lupus erythematosus, Multiple Sclerosis, Graves' Disease) that require treatment with an immune modulator treatment or anti-inflammatory medication

12. Surgical operations to the mouth or gastrointestinal tract within 4 weeks prior to study entry, or planned during the study

o Appendectomy within 6 months prior to study entry

13. Recent unintended weight loss:

o >5% of total body weight within 6 months prior to study entry

14. Excessive alcohol consumption (>14 units per week) and/or drug abuse

15. Pregnancy and lactation, or plan to become pregnant during the study period

16. Participation in other studies involving investigational or marketed products concomitantly or within 3 months prior to study entry

17. Changes in diet, supplement or medication use likely to affect study outcomes (i.e. medication that influences GI function) within 4 weeks prior to study entry or planned during the study (at the discretion of the Investigator). For example, the following medications will influence GI function and changes must be avoided: opioids, prokinetics (domperidone, metoclopramide, prucalopride), antispasmodics (peppermint oil, buscopan), and acid suppressants (PPI, H2 blockers). Of note: the intake of fibres (e.g. psyllium husk) may be used provided that the participant has been using this as a supplement for more than 4 weeks prior to study participation and intake does not change during the course of participation.

Related Conditions & MeSH terms

• Constipation
• Diarrhea
• Irritable Bowel Syndrome
• Syndrome

Intervention

Dietary Supplement:
• Galacto-oligosaccharides (GOS)
An 8-week intervention study, preceded by a 2-week run-in period, in which a daily dose of a prebiotic supplement is given to adult patients diagnosed with IBS (diarrhoea, constipation or mixed-type). Patients need to report several symptom experiences and blood and faecal samples are collected.
• Maltodextrine
An 8-week intervention study, preceded by a 2-week run-in period, in which a daily dose of a placebo is given to adult patients diagnosed with IBS (diarrhoea, constipation or mixed-type). Patients need to report several symptom experiences and blood and faecal samples are collected.

Locations

Country	Name	City	State
Belgium	University Hospital Leuven location Gasthuisberg	Leuven
Netherlands	Jeroen Bosch Ziekenhuis, Gastroenterology department	's-Hertogenbosch	Noord-Brabant
Netherlands	Ziekenhuis Gelderse Vallei, Afdeling Maag-Darm-Leverziekten	Ede
Netherlands	Medisch Centrum Leeuwarden (MCL)	Leeuwarden	Friesland
United Kingdom	County Durham &Darlington NHS Foundation trust, University Hospital of North Durham	Durham
United Kingdom	Leeds Teaching Hospital NHS Trust in association with the University of Leeds	Leeds	North Yorkshire
United Kingdom	Barts Health NHS Trust, Wingate Clinical Trials Facility	London
United Kingdom	Manchester University NHS Foundation Trust, Wythenshawe Hospital, Neurogastroenterology Unit	Manchester
United Kingdom	NIHR National Patient Recruitment Centre Newcastle	Newcastle Upon Tyne

Sponsors (2)

Lead Sponsor	Collaborator
Clasado	CR2O B.V.

Countries where clinical trial is conducted

Belgium,  Netherlands,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Immune function	The difference in immune function between treatment arms as determined by blood markers of immune function.	At the end of the study (Day 56).
Other	Gut microbiome composition	The difference in gut microbiome composition between treatment arms as determined by faecal metagenomics.	At the end of the study (Day 56).
Other	Blood metabolites	The difference in blood metabolites between treatment arms as determined by blood metabolomic analysis.	At the end of the study (Day 56).
Other	Correlation between blood metabolites and gut microbiome	The correlation of blood metabolites and gut microbiome in both treatment arms, and the difference between arms.	At the end of the study (Day 56).
Other	Correlation between gut microbiome and mean composite IBS-Symptom Severity Scores	The correlation of gut microbiome and mean composite IBS-Symptom Severity Scores in both treatment arms, and the difference between arms.	At the end of the study (Day 56).
Primary	IBS symptom Severity	The difference in total IBS symptom severity between treatment arms as measured by mean composite IBS Symptom Severity Scale scores. The IBS System Severity Scores Scale consists of 5 questions each with scales ranging from 0 to 100, divided into steps of 10, whereby a score of 0 reflects the best outcome, and a score of 100 reflects the worst outcome.	Baseline to end of the study (Day 56).
Secondary	Abdominal pain	The difference in abdominal pain between treatment groups as measured by the mean abdominal pain symptom scores as reported by patients in their electronic diaries. Patients are requested to rate their worst abdominal pain over the past 24 hours on a scale from 0 = no abdominal pain, 10 = worst possible abdominal pain.	During the intervention period (8 weeks)
Secondary	Bloating.	The difference in bloating between treatment groups as measured by the mean bloating symptom scores as reported by patients in their electronic diaries. Patients are requested to to rate their worst bloating symptoms over the past 24 hours, on a scale from 0 = no bloating, 10 = worst possible bloating.	During the intervention period (8 weeks)
Secondary	Global IBS improvement	The difference in global IBS improvement between treatment arms as measured by the mean IBS Global Improvement Scale scores. Patients are requested to rate their IBS signs or symptoms overall over the past 7 days on a scale from 1 = significantly relieved to 7 = significantly worse.	During the intervention period (8 weeks)
Secondary	Stool consistency	The difference in stool consistency between treatment arms, per subtype of IBS**, as measured by the median Bristol Stool Form Scale stool type. The Bristol Stool Form Scale stool types vary from 1 (separate hard lumps) to 7 (watery, no hard pieces). Normal stools would be rated in the middle of this scale (3, 4, or 5)	During the intervention period (8 weeks)
Secondary	Defecation frequency	The difference in defecation frequency between treatment arms, per subtype of IBS**, as measured by the mean patient-reported defecation frequency.	During the intervention period (8 weeks)
Secondary	Quality of Life IBS-QOL score	The difference in quality of life between treatment arms as measured by the mean composite IBS Quality of Life scores. The IBS Quality of Life validated questionnaire offers patients 34 statements concerning bowel problems (Irritable Bowel Syndrome, IBS) and how these affected the patient over the past 30 days, Scores range from 1 (not at all) to 5 (extremely)	At the end of the study (Day 56)
Secondary	Anxiety and depression	The difference in anxiety and depression between treatment arms, evaluated separately using the mean IBS Hospital Anxiety and Depression Scale scores. The Hospital Anxiety and Depression scale asks patients to rate how they feel in 14 questions, each offering 4 different outcomes ranging from the best possible feeling to worst possible feeling	At the end of the study (Day 56)
Secondary	Nature, incidence, frequency, severity of adverse events/serious adverse events and relationship to the study intervention.	To assess the safety of treatment with GOS in patients with IBS	During the intervention period (8 weeks)
Secondary	Rescue medication	Difference in use of rescue medication between treatment arms	From screening to end of intervention period (10 weeks)