Effect of Two Different Rye Bread Types in Irritable Bowel Syndrome
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ClinicalTrials.gov Identifier: NCT02161120 |
Recruitment Status :
Completed
First Posted : June 11, 2014
Last Update Posted : March 31, 2015
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Condition or disease | Intervention/treatment | Phase |
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Irritable Bowel Syndrome | Other: Traditional Finnish rye bread Other: Low FODMAP rye bread | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 87 participants |
Allocation: | Randomized |
Intervention Model: | Crossover Assignment |
Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Effects of Traditional and Low-FODMAP Rye Bread in Irritable Bowel Syndrome. |
Study Start Date : | April 2014 |
Actual Primary Completion Date : | February 2015 |
Arm | Intervention/treatment |
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Active Comparator: Traditional rye bread
As part of habitual diet participants are expected to consume 100-200 grams of traditional Finnish rye bread daily
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Other: Traditional Finnish rye bread |
Experimental: Low-FODMAP rye bread
As part of habitual diet participants are expected to consume 100-200 grams of low-FODMAP rye bread daily
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Other: Low FODMAP rye bread |
- Change is IBS symptoms by using IBS-SSS questionaire [ Time Frame: 4 weeks ]
- IBS quality of life by using IBS QoL questionnaire [ Time Frame: 4 weeks ]
- Changes in specific IBS symptoms measured by 100 mm VAS scale [ Time Frame: 4 weeks ]
- Changes is intestinal microbiota evaluated by fecal samples [ Time Frame: 4 weeks ]
- Changes in hydrogen excretion evaluated by 6 hours breath test after standard rye bread breakfast [ Time Frame: 4 weeks ]

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Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- IBS according to Rome III criteria. Accepted sub-types include IBS-M, IBS-D and IBS-U
- Age 18-65 years
- Willing to use rye bread daily during the study periods
Exclusion Criteria:
- IBS-C (constipation dominant)
- Celiac disease
- IBD
- Major gastrointestinal operations like bowel gastric resection
- Non-treated hypo- or hyperthyroidism
- Alcoholism, severe depression, dementia, cancer or other diseases likely to severly impair the participants ability to conclude the protocol
- Regular (almost daily) use of NSAIDs, antibiotics or lactulose
- Linaclotide and other prescription medicines targeted specifically to IBS
- Pregnancy and lactation
- Follows currently strict low-FODMAP diet

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02161120
Finland | |
Aava Medical Centre | |
Helsinki, Finland, 00100 |
Responsible Party: | Oy Karl Fazer Ab |
ClinicalTrials.gov Identifier: | NCT02161120 |
Other Study ID Numbers: |
BSTN-2014-rye |
First Posted: | June 11, 2014 Key Record Dates |
Last Update Posted: | March 31, 2015 |
Last Verified: | March 2015 |
IBS, irritable bowel syndrome, functional gastrointestinal disorder, diet, bread, rye, FODMAP, microbiota |
Irritable Bowel Syndrome Syndrome Disease Pathologic Processes Colonic Diseases, Functional |
Colonic Diseases Intestinal Diseases Gastrointestinal Diseases Digestive System Diseases |