Irritable Bowel Syndrome Clinical Trial
— PROALIFUNOfficial title:
Effect of Wheat Bread and Pasta With Reduced Content of Gluten on Patients With Irritable Bowel Syndrome: Randomized Controlled Cross Over Study
Verified date | August 2018 |
Source | University of Bari |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study aim to manufacture bread and pasta with an reduced content of gluten and to assess the impact of reducing the daily intake of gluten by 50% in irritable bowel syndrome (IBS) patients. Fungal proteases and selected sourdough lactic acid bacteria will be used for making wheat bread and pasta with a reduced content of gluten (RG) (-50% of traditional products). From a technological point of view, the chemical, structural and sensory features of the RG products approached those of the bread and pasta made with normal level of gluten. The efficacy and safety of new products will be compared to traditional bread and pasta by using a double blind randomized, crossover-controlled trial in IBS patients with persistent gastrointestinal symptoms. Patients will follow two weeks of a GFD diet containing RG bread and pasta and two weeks of GFD diet containing Normal Gluten bread and pasta Symptoms severity will be assessed by Irritable Bowel Syndrome Severity Score (IBS-SS), Visual Analogue Scale (VAS), Hospital Anxiety and Depression Scale (HADS) and Irritable Bowel Syndrome Quality of Life (IBS-QoL).
Status | Completed |
Enrollment | 20 |
Est. completion date | December 31, 2017 |
Est. primary completion date | December 31, 2016 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. age above 18 years; 2. having bowel symptoms (altered bowel habit, lower abdominal pain, bloating, or distention suggestive of IBS), as determined by Rome III criteria. 3. Previous exclusion of CD and wheat allergy Exclusion Criteria: 1. previous GI malignancy and/or surgery; 2. clinically significant cardiovascular, respiratory, endocrine, renal, hematologic or hepatic disease. 3. other clinically significant medical condition; pregnancy or lactation; alcohol abuse; drug addiction; severe neurologic or psychiatric disorders; long-term use of corticosteroids or anti-inflammatory drugs 4. participation in another clinical trial within 6 months before the onset of this trial. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University of Bari |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Severity of IBS symptoms measured by Irritable Bowel Syndrome-Severity Score (IBS-SS) | Change in IBS Severity Score (IBS-SS) between reduced gluten content diet and standard gluten content diet. Mild, moderate and severe cases were indicated by scores of 75 to 175, 175 to 300 and "300 respectively. Mild, moderate and severe cases are indicated by scores of 75 to 175, 175 to 300, and >300, respectively. | two weeks of each different diet interspersed by one week of wash out. The questionnaire will be completed ones a week. | |
Primary | Change of IBS severity measured by Visual analogue scale (VAS) | Change of severity of IBS symptoms measured by Visual analogue scale (VAS) between reduced gluten content diet and standard gluten content diet. The 0-10 mm VAS scale (0 no pain, 10 worst possible pain) included a horizontal color gradient (green-red). | Two weeks of each different diet interspersed by one week of wash out. The scale will be completed ones a day. | |
Secondary | Change of Quality of life scores | Irritable Bowel Syndrome Quality of Life (IBS-QoL) between reduced gluten content diet and standard gluten content diet. | two weeks of each different diet interspersed by one week of wash out. The scale will be completed ones a week. |
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