Human Milk Oligosaccharides (HMOs) for Irritable Bowel Syndrome (IBS)

Irritable Bowel Syndrome Clinical Trial

— HIBS  

Official title:

Supporting Healthy Gastrointestinal Function With Human Milk Oligosaccharides (HMOs) in Individuals With Irritable Bowel Syndrome (IBS)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05205785
• Other study ID #: 2021-07-21-HMOS
• Status: Recruiting
• Phase: N/A
• Start date: March 22, 2023
• Est. completion date: January 2025

Study information

• Verified date: February 2023
• Source: DSM Nutritional Products, Inc.
• Contact: Aisling Harrington
• Phone: +353 21 430 7442
• Email: aharrington[@]atlantiatrials.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To assess the effects of a Human Milk Oligosaccharide mix given once daily for 12 weeks on stool consistency and abdominal pain compared to placebo in individuals with Irritable Bowel Syndrome (IBS).

Description:

HMO mix has been shown to provide therapeutic benefits to individuals with IBS of all subtypes (Palsson et al., 2019). DSM is planning this trial in order to investigate if clinically relevant improvements in bowel movements and IBS symptoms can be obtained through the use of the HMO mix in individuals with moderate to severe IBS and abdominal pain. Eligible participants will have a diagnosis of Irritable Bowel Syndrome (IBS). Participants will be assessed for eligibility at the screening visit, must meet all the inclusion criteria, and none of the exclusion criteria. In this trial, participants will be randomized to one of two intervention groups (a Human Milk Oligosaccharide mix or placebo) and receive intervention for at least 12 weeks.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 500
• Est. completion date: January 2025
• Est. primary completion date: February 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Written informed consent obtained before any trial related assessments are performed.

2. Male or female aged =18 years at the time of consent. a. Female participants of child-bearing potential (females who are post-menopausal, i.e., when there has been no menstruation for a minimum of 12 months prior to screening, are considered not to be of child-bearing potential.), who are not surgically sterilized, must have a negative pregnancy test at screening and be willing to practice one of the following appropriate contraceptive methods until the last visit: i. Sexual abstinence. ii. Oral contraceptives. iii. Trans dermal patches or depot injection of a progestogen drug (starting at least 4 weeks prior to product administration). iv. Double barrier method: condom or occlusive cap (diaphragm or cervical/vault caps) plus spermicidal agent. v. Intrauterine device (IUD), intrauterine system (IUS), subdermal implant, or vaginal ring (placed at least 4 weeks prior to product administration). vi. Contraceptives must be effective before the randomization visit. However, national requirements should always be followed.

3. IBS-D or IBS-C or IBS-M according to Rome IV criteria. This will be established by using the IBS Module of the Rome IV Diagnostic Questionnaire, and requires recurrent abdominal pain on average at least 1 day per week during the previous 3 months that is

associated with two or more of the following:

1. Related to defecation (may be increased or unchanged by defecation) on at least 30% of pain instances in past 3 months.

2. Associated with a change in stool frequency (on at least 30% of pain instances in past 3 months).

3. Associated with a change in stool form or appearance (on at least 30% of pain instances in past 3 months).

4. Reported IBS diagnosis from a physician.

5. Personal access to the internet via computer, tablet, or smart-phone.

6. Be willing and able to comply with trial protocol, including entry of electronic diary data for at least 12 out of 14 diary days during the pre-randomization baseline 2-week run-in diary period (between V1 andV2). Inclusion criteria Visit 2: To be eligible for inclusion, the participant must fulfil

all of the following criteria:

7. Scores of 1, 2, 6, or 7 on the Bristol stool scale at least twice per week [as determined by eDiary completion between V1 and V2].

8. An average baseline of worst abdominal pain of =3.3 (NRS-11) during the 2-week run-in period prior to randomization [as determined by eDiary completion between V1 and V2]. Exclusion Criteria: The presence of any of the following criteria will exclude the participant from

participating in the trial:

1. Treatment with an investigational drug from another clinical trial within 30 days/5 half- lives of the drug (which ever longest) prior to screening visit.

2. Any known gastrointestinal disease(s) or medical history that may interfere with the

trial evaluations in the opinion of the investigator, in particular:

1. Coeliac disease.

2. IBD.

3. Diverticulitis.

4. C. difficile infection reported in the previous 2 years.

5. Any clinically symptomatic biochemical or structural abnormality or active disease of the gastrointestinal tract within 6 months before screening, including daily diarrhea within two weeks prior to the screening interview or during the screening/baseline period.

6. Substance abuse (within past 2 years).

7. New use of antibiotics (within past 2 months), prebiotics, probiotics, or fiber supplements (within the past month).

8. Hepatic dysfunction assessed as part of the blood safety panel (defined as alanine aminotransaminase/serum glutamic-pyruvic transaminase or aspartate aminotransaminase/serum glutamic-oxaloacetic transaminase >2.5 x the upper limit of normal, or a history of hepatobiliary disease) or renal impairment (serum creatinine) >2 mg/dl); any surgery (within a year of screening) on the stomach, small intestine, or colon (excluding appendectomy, hernia surgery not involving the GI tract, or c-section).

9. Any history of pancreatitis (either acute or chronic).

10. Laxative abuse (use of more than recommended dosage).

11. Pregnant or lactating individuals.

12. Any other gastrointestinal disease(s) or medical history that may interfere with the trial evaluations in the judgment of the investigator.

3. Following strict diets to improve their IBS symptoms as judged by the investigator e.g., Low FODMAP (within past 2 months). Exclusion based on diet will be reviewed by single investigator for consistency.

4. Any clinically relevant chronic disease(s) such as malignancy, diabetes, severe coronary disease, kidney disease, autoimmune or neurological disease, that in the opinion of the investigator would interfere with the trial evaluations or the safety of the participant.

5. Current severe psychiatric disease and/or psychological disturbance, a major psychiatric disorder requiring hospitalization in the last 3 years, or a history of attempted suicide or uncontrolled bipolar disorder; or clinical evidence of any significant psychiatric disease or symptoms that may interfere with the participant successfully completing the trial.

6. Treatment with restricted and prohibited concomitant medications.

7. Diagnosed with and treated for IBS for more than 10 years

8. Has a business or personal relationship with trial staff or sponsor who is directly involved with the conduct of the trial.

9. Lack of suitability for participation in the study for any reason as judged by the investigator.

10. Has previously been randomized into this trial, is participating in this trial at another investigational site or is planning to participate in any other clinical trial during this trial.

11. Desire and/or plans on changing current diet regime during the participation of this trial.

Related Conditions & MeSH terms

• IBS - Irritable Bowel Syndrome
• Irritable Bowel Syndrome
• Syndrome

Intervention

Dietary Supplement:
• Human Milk Oligosaccharide Mix
Subjects takes 5.5 g of powder mixed in water once a day for 12 weeks.

Other:
• Placebo
The placebo to be used in this trial is 5.5 g of powdered dextrose powder in a single-serve stick pack. The participants will be instructed to mix the product in a 4-6 oz glass of water and consume in the morning once a day for 12 weeks.

Locations

Country	Name	City	State
Ireland	Atlantia Clinical Trials Ltd	Cork	Cork/Munster

Sponsors (1)

Lead Sponsor	Collaborator
DSM Nutritional Products, Inc.

Country where clinical trial is conducted

Ireland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Absolute change in GSRS-IBS (Gastrointestinal Symptom Rating Scale-IBS) scores.	The Gastrointestinal Symptom Rating Scale- Irritable Bowel Syndrome questionnaire contains 13 items, each uses a seven-graded Likert scale, where 1 represents the most positive option (no symptoms) and 7 the most negative one (severe symptoms). The participant will answer each question with respect to their experience over the last 7 days. To calculate the Total Score, each of the 13 item scores will be used to calculate a mean Total Score: minimum possible score = 0; maximum possible score = 7; higher scores indicate worse symptoms.; A mean value for the items in each dimension (Diarrhea; Constipation; Bloating; Pain & Satiety) will be calculated: minimum possible score = 0; maximum possible score = 7; higher scores indicate worse symptoms.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Abdominal pain responder rate.	Based on the proportion of participants with a decrease in weekly average of worst abdominal pain of at least 30%.	Baseline (2-week run-in period) to the last two weeks of intervention (week 11+12)
Other	Absolute change in BSFS (Bristol Stool Form Scale) score.	Participants will identify each bowel movement 'type' using the Bristol Stool Scale (Type 1 = hard stool difficult to pass [classified as severe constipation]; Type 7 = watery, entirely liquid stool [classified as severe diarrhea]). Lower scores are indicative of constipation, and higher scores are indicative of diarrhea.	Baseline (2-week run-in period) to the last two weeks of intervention (week 11+12)
Other	Absolute change in the number (or frequency) of bowel movements.	Participants will report number of daily bowel movements. This endpoint will compare the change in number of bowel movements from baseline to end of intervention.	Baseline (2-week run-in period) to the last two weeks of intervention (week 11+12)
Other	Percentage of participants with a decrease of 50 points in total IBS-SSS score.	The IBS Symptom Severity Scale (IBS-SSS) contains 5 items. Each of the five questions generate a maximum score of 100 using prompted visual analogue scales. The maximum achievable score is 500 with a decrease in score indicating a decrease in the severity of symptoms.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Absolute change in GAD-7 score.	The General Anxiety Disorder 7-item questionnaire (GAD-7) is a 7 item scale, each uses a four-graded Likert scale, where 0 represents the 'not at all' and 3 represents 'nearly every day'. The maximum score is 21 and scores of 5, 10, and 15 are taken as the cut-off points for mild, moderate and severe anxiety, respectively.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Absolute change in PHQ-8 score.	The Patient Health Questionnaire 8 (PHQ-8) is an 8 item scale. Each uses a four-graded Likert scale, where 0 represents 'not at all' and 3 represents 'nearly every day' and asks the participant how often (over the past two weeks) they have been bothered by each item. A total score of 0 to 4 represents no significant depressive symptoms; 5 to 9 represents mild depressive symptoms; 10 to 14, moderate symptoms; 15 to 19, moderately severe symptoms; and 20 to 24, severe symptoms.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Absolute change in WPAI-IBS (Work Productivity and Activity Impairment-IBS) score.	Absolute change measured by the WPAI-IBS.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Absolute change in BIPQ score.	The Brief Illness Perception Questionnaire (BIPQ) is a nine-item scale designed to assess the cognitive and emotional representations of illness. All of the items except the causal question (item 9) are rated using a 0 (most negative) to 10 (most positive) response scale from total score is calculated.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Absolute change in total IBS-SSS score and individual scores.	The IBS Symptom Severity Scale (IBS-SSS) contains 5 items. Each of the five questions generate a maximum score of 100 using prompted visual analogue scales. The maximum achievable score by an individual is 500.	Baseline (Visit 2) to week 4 (call 1), to week 8 (call 2), and to week 12 (Visit 3)
Other	Absolute change in the use of medications and treatments for bowel habits.	Participants will report daily use of medications and treatments for bowel habits	Baseline (2-week run-in period) to the last two weeks of intervention (week 11+12).
Other	Adverse Events by product causality	Proportion of AEs per group by product causality	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Incidence of mild, moderate, and severe AEs	Incidence of mild, moderate, and severe AEs per group by product causality.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Severe Adverse Events (SAEs) by product causality	Incidence of SAEs per group by product causality	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Vitals I	Change in systolic blood pressure (mmHg)	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Vitals II	Change in diastolic blood pressure (mmHg)	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Vitals III	Change heart rate (bpm)	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Vitals IV	Change temperature (degrees °F)	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Safety Labs	This outcome will report the incidence of 'out of range' blood safety parameters assessed from a standard safety chemistry panel and a standard safety hematology panel (Full Blood Count). 'Out of range' is determined based on clinically defined 'normal' ranges for each analyte. A higher incidence of 'out of range' blood safety parameters would be a worse safety outcome in this case.	Baseline (Visit 2) to Week 12 (Visit 3)
Other	Urinalysis (pH, protein, glucose, ketone, urobilinogen, bilirubin, blood, and nitrite).	This outcome will report the incidence of 'out of range' Urinalysis safety parameters (pH, protein, glucose, ketone, urobilinogen, bilirubin, blood, and nitrite). 'Out of range' is determined based on clinically defined 'normal' ranges for each analyte. A higher incidence of 'out of range' urinalysis safety parameters would be a worse safety outcome in this case.	Baseline (Visit 2) to Week 12 (Visit 3)
Primary	Absolute change in the proportion of stools with abnormal fecal consistency in the active product compared to placebo group.	Participants will identify each bowel movement 'type' using the Bristol Stool Scale (Type 1 = hard stool difficult to pass [classified as severe constipation]; Type 7 = watery, entirely liquid stool [classified as severe diarrhea]). Types 1 and 2 would be considered to suggest severe and mild diarrhea, respectively. Types 6 and 7 would be considered to suggest mild and severe diarrhea, respectively. This endpoint will compare the proportion of participants experiencing constipation and diarrhea between the groups	Baseline (2 week run in period) to end of intervention (weeks 11 + week 12)
Primary	Absolute change in the pain severity score (IBS-SSS) in the active product compared to placebo group.	The IBS Symptom Severity Scale (IBS-SSS) contains a pain subscale which asks participants to rate abdominal pain the past 10 days on a scale from 0 to 100, with 0 meaning "no pain" and 100 meaning "very severe pain". The minimum score is 0 and the maximum achievable score is 100.	Baseline (Visit 2) to Week 12 (Visit 3)
Secondary	Absolute change in total IBS severity score in the active product compared to placebo group.	The IBS Symptom Severity Scale (IBS-SSS) contains 5 items. Each of the five questions generate a maximum score of 100 using prompted visual analogue scales. The minimum score is 0 and the maximum achievable score is 500.	Baseline (Visit 2) to Week 12 (Visit 3)
Secondary	Absolute change in total IBS Quality of Life (IBS-QOL) score in the active product compared to placebo group.	The IBS Quality of Life contains 34 items each with a five-point response scale, where 1 represents not at all and 5 extremely/A great detail. The participant ill answer each question with respect to the impact of IBS and it's treatment. The individual responses to the 34 items are summed and averaged for a total score and transformed to a 0-100 scale for interpretation with higher scores indicating better IBS specific quality of life.	Baseline (Visit 2) to Week 12 (Visit 3)
Secondary	Relative change in abundance of fecal Bifidobacteria spp in the active product compared to placebo group.	Relative change in abundance measured by gene sequencing analysis of fecal sample.	Baseline (Visit 2) to Week 12 (Visit 3)