Irritable Bowel Syndrome is a common disease to which there is no curable treatment. Diet is considered to trigger symptoms associated with the clinical picture of IBS, and dietary treatment is thus believed to relieve the symptoms of IBS. As the disease is very heterogeneous in its manifestation, different treatment options might be indicated depending on the predominant symptom. To investigate the response to different dietary treatment options, a randomized controlled intervention trial will be carried out in adult patients (\>18 y) with IBS according to Rome IV criteria. The aim of this study is to compare the response to two different dietary treatments or optimized medical treatment.
The study is a randomized controlled trial comparing three different treatments during four weeks: 1. Combination of low FODMAP diet + traditional dietary advice (based on NICE recommendations) * Eat at regular hours; 3 main meals and 3 snacks * Eat in peace, chew the food properly * Peel all fruits and vegetables * Limit intake of spicy and fatty foods, coffe, alcohol, avoid fizzy drinks and chewing gum * Choose soluble rather than insoluble fibres * Avoid foods high in FODMAPs 2. Diet low in carbohydrates * 10 E% carbohydrates, 23 E% protein, 67 E% fat * Larger amounts of fish, shellfish, meat, egg, dairy products (lactose free if wanted) nuts, seeds, oil, vegetables * No sugary or starchy foods, e.g pasta, potatoes, bread, rice, most fruits * No specific consideration about FODMAP content 3. Optimized pharmacological tretament based on predominant symptom and previous experience with pharmacological treatmment. Pain/discomfort: * Pain: Amitriptyline 25 mg. Increase to 50 mg if needed * Episodic pain: Hyoscyamine 0,2mg 2x2; adjust dose if needed * Pain with diarrhea: Amitriptyline 25 mg. Increase dose if needed * Pain with constipation: Linaclotide 290 microgram 1x1 Constipation: * Bulking agent (Sterculia gum (Inolaxol) 1x1. Increase to 1x3 if needed * Osmotic laxative (Macrogol (Movicol) 1x1 * Linaclotide 290 microgram 1x1 Diarrhea * Loperamide 1x2 . Adjust dose if needed * Cholestyramine 1x1. Increase ever 3-5 d as needed * Ondansetron 4mg 1x1. Increase to 1x2-3 if needed * Eluxadoline 100mg 1x2 Primary endpoint: IBS-SSS reduction \>50 points
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Enrollment
300
Traditional dietary advice according to the Brittish Dietetic Association including reducing the intake of fermentable carbohydrates.
Diet that contains a maximum of 10 energy percent of carbohydrates, 23 energy % proteins and 67 energy % fat.
Standard consultation by physician and if needed patients will receive medical treatment based on the most prominent symptom. Constipation: osmotic laxatives, linaclotide. Diarrhea: loperamid, bile acid binders. Pain: anti depressent, antispasmodics, linaclotide.
Magnus Simren
Gothenburg, Non-US/Non-Canadian, Sweden
The proportion (%) of patients who respond to treatment
A responder is defined as having an IBS-SSS reduction \>50 points @ 4 weeks
Time frame: Baseline to 4 weeks
Change in symptom severity
Absolute and percentage change in IBS-SSS
Time frame: Baseline, 4 weeks, 3 and 6 months
Determinants for GI symptoms by IBS-SSS
GI symptoms measured by IBS-SSS
Time frame: Baseline, 4 weeks, 3 and 6 months
Determinants for GI symptoms by GSRS-IBS
GI symptoms measured by GSRS-IBS
Time frame: Baseline, 4 weeks, 3 and 6 months
Predictors of response to treatment
Potential predictors include demographics, questionnaire data, microbiota, metabolites, immunology
Time frame: Baseline to 4 weeks
Adherence to allocated intervention
Including compliance to dietary intervention during 4 weeks, and long-term adherence during follow-up
Time frame: Baseline, 4 weeks, 3 and 6 months
Change in microbiota content
Fecal microbiota analysis using 16S technique
Time frame: Baseline, 4 weeks, 6 months
Change in extra-intestinal symptoms and quality of life
As assessed by IBS specific questionnaires
Time frame: Baseline, 4 weeks, 3 and 6 months
Change in metabolic profile
Metabolomics in serum and urine samples
Time frame: Baseline, 4 weeks, 6 months
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