Irritable Bowel Syndrome Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with irritable bowel syndrome (IBS)
- People who have already had genetic testing related to genes that control the production of certain digestive enzymes (called sucrase-isomaltase), as part of a previous study involving a low-starch and low-sugar diet (called SSRD) or a related multi-centre study
Who may not be able to join:
- People who have been diagnosed with inflammatory bowel disease, coeliac disease, bile salt malabsorption, gastroenteritis, or problems with how the gut moves food through the body
- People who have a severe food allergy
- People who have a serious heart, lung, cardiovascular, or mental health condition, or a serious illness such as cancer
- People who currently have an eating disorder
- People who are pregnant
- People who have recently had major surgery on their digestive system
- People who have an addiction to alcohol or drugs
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Cecilia Kennbäck, Registered Nurse, Department of Internal Medicine, Skåne University Hospital, 20502 Malmö
Phone: +46+402712660
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Changes of blood glucose after a meal intake
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.