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| Name | Class |
|---|---|
| Chr Hansen | INDUSTRY |
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The purpose of this study is to investigate if the probiotic Bifidobacterium breve Bif195 (Bif195) will result in improvement in clinical outcome in patients with diarrhea-predominant irritable bowel syndrome (IBS).
IBS is the most frequently diagnosed gastrointestinal disease and also the most common cause of referrals to gastroenterology departments in Denmark.
The possibilities for treatment for IBS are limited. Treatment strategies that involve the microbiota provide symptom relief in some IBS patients. Several studies have demonstrated that the composition of the gut microbiota in IBS patients is different from healthy controls.
Probiotic interventions has shown promising results, but it currently remains unknown which probiotics are effective and which are not.
A new probiotic bacterium, Bifidobacterium breve Bif195 (Bif195) has been identified and has shown great effects on preventing enteropathy and ulcers on the gut mucosa in healthy volunteers given acetylsalicylic acid, and thereby Bif195 has also shown a potential in reducing gut permeability defects. This bacterium has not yet been investigated in IBS patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Bif195 capsules | Active Comparator | The capsule will contain approximately 15*10^9 CFU of Bif195 per day. Excipients: Microcrystalline Cellulose 6 mg per capsule, Magnesium Stearate 1.5 mg per capsule, Maltodextrin 277.8 mg per capsule, and Sodium Ascorbate 14.7 mg per capsule. |
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| Placebo capsules | Placebo Comparator | The capsule contain only excipients: Microcrystalline Cellulose 6 mg per capsule, Magnesium Stearate 1.5 mg per capsule, Maltodextrin 277.8 mg per capsule, and Sodium Ascorbate 14.7 mg per capsule. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Bifidobacterium breve Bif195 | Dietary Supplement | 1 capsule daily for 8 weeks |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Change in IBS symptoms from baseline measured by IBS-severity scoring system (IBS-SSS) at 8 weeks | IBS-SSS is a composite score of abdominal pain, number of days with abdominal pain, bloating/distension, satisfaction with bowel habits, and IBS-related quality of life. Each measure is rated from 0 to 100, with total scores ranging from 0 (best) to 500 (worst). | 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in quality of life from baseline measured by Irritable Bowel Syndrome-Quality of Life (IBS-QOL) Questionnaire Scores at 8 weeks | The IBS-QoL questionnaire consists of 34 items, each with a 5-point response scale. The 34 items are based on the following eight variables: health worries, food avoidance, body image, dysphoria, interference with activity, social reactions, sexual activity and relationships. The IBS-QoL score will be transformed into a 0-100 scale using the formula: total score = (sum of the items-34/170) ×100. Low score (best) |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hvidovre Hospital, Copenhagen University | Hvidovre | Copenhagen | 2650 | Denmark | ||
| Copenhagen University Hospital Hvidovre |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 41648756 | Derived | Gronbaek IMB, Halkjaer SI, Hansen EH, Mollerup S, Paulsen SJ, Konrad CV, Engel S, Bulinska-Balas M, Wellejus A, Haaber AB, Christensen AH, Engsbro AL, Petersen AM. Eight weeks of treatment with probiotic Bifidobacterium breve, Bif195 lowers fatigue scores in patients with diarrhoea-predominant irritable bowel syndrome: results from a randomised, clinical trial. Front Nutr. 2026 Jan 21;12:1701341. doi: 10.3389/fnut.2025.1701341. eCollection 2025. |
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| ID | Term |
|---|---|
| D043183 | Irritable Bowel Syndrome |
| ID | Term |
|---|---|
| D003109 | Colonic Diseases, Functional |
| D003108 | Colonic Diseases |
| D007410 | Intestinal Diseases |
| D005767 | Gastrointestinal Diseases |
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| Placebo |
| Dietary Supplement |
1 capsule daily for 8 weeks |
|
| 8 weeks |
| Changes from baseline in bowel habits at 8 weeks | measured by frequency/day and Bristol Stool Form Scale. The Bristol Stool Form Scale is divided into seven categories were a low value indicate constipation and a high value indicate diarrhoea. | 8 weeks |
| Change from baseline in abdominal pain at 8 weeks | Measured by a VAS scale from 0-10. 0 = no pain, 10 = worst pain | 8 weeks |
| Adverse events | Reported according to IHC-GCP | 16 weeks |
| Hvidovre |
| 2650 |
| Denmark |
| D004066 | Digestive System Diseases |