- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02761785
Gluten-free Oats and Gastrointestinal Health in Coeliac Disease, Part 2
The research aims to investigate the effects of gluten-free oats to the gastrointestinal health in celiac disease patients and healthy subjects. The effects of gluten-free oats on the several intestinal parameters, on the composition of the gut microbiota as well as on the metabolic profile of celiac patients and healthy controls will be studied. The study is divided into two parts.
Part 1 will be conducted as a double-blind, randomized and placebo-controlled cross-over study. Healthy subjects will be recruited to the study. The aim is to recruit 15 participants for the part 1. The study will be conducted with a cross-over setting, where the subjects will go through exposure meals and SmartPill ingestion three times (two different oat products and placebo) in a randomized order. The study meals are identical in appearance and fiber content. After consuming the meal subjects will ingest the SmartPill capsule, which will send data on intestinal pH, pressure and temperature to the external portable device. Before and during the passage of capsule the subjects will fill a symptom and food diary. The capsule will exit the body in 1 to 3 days and the data collected by the external device will be collected and analyzed. Before the oat/placebo exposure the subjects will give a fecal and a blood sample. In addition, 36 hours urine samples will be collected.
In part 2 celiac disease patients, non-celiac gluten sensitive subjects and healthy controls will be recruited and they will be divided into four groups: oat-avoiding celiacs (1), oat-consuming celiacs (2), non-celiac gluten sensitive subjects (3) and healthy controls (4). Recruiting aim for each group is 15 subjects. In addition to dietary data, a blood, and a fecal sample will be collected from the subjects. The gut microbiota will be analyzed from the fecal samples. The metabolic products will be analyzed from the fecal, urine and blood samples. The gut microbiota composition will be analyzed with next-generation DNA sequencing techniques.
Study Overview
Status
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Turku, Finland, 20014
- Department of Biochemistry, University of Turku
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Group 1:Celiac patients who have self-reported gastrointestinal symptoms after ingestion of gluten-free oats
Group 2: Celiac patients who include gluten-free oats in their diet and have no symptoms related to oats
Group 3: Non-celiac gluten sensitive subjects
Group 4: Healthy controls (without celiac disease) who include oats in their diet
Description
Inclusion Criteria:
- Celiac disease diagnosed with duodenal biopsy (only celiac groups)
- In remission and maintained gluten-free diet >1 year (only celiac groups)
- Usage of oats in their diet (only oat-using celiacs and healthy controls)
- BMI 18,5 - 30
- Normal liver, thyroid and kidney functions
Exclusion Criteria:
- Medication that majorly affects GI tract (e.g. laxatives, antacids)
- Antibiotic treatment within the last 6 months
- Blood donation or participating in another clinical trial within the last month
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Celiacs with oat-related symptoms
Celiac patients who have self-reported gastrointestinal symptoms after ingestion of gluten-free oats
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Celiacs without oat-related symptoms
Celiac patients who include gluten-free oats in their diet and have no symptoms related to oats
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Healthy controls
Healthy controls (without celiac disease) who include oats in their diet
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Non-celiac gluten sensitive subjects
Subjects with manifestations precipitated by ingestion of gluten in whom celiac disease and wheat allergy are excluded.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Fecal microbiota composition
Time Frame: Measured from single time point sampling
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Fecal microbiota diversity and composition analyzed from fecal sample
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Measured from single time point sampling
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Metabolic status
Time Frame: Measured from single time point sampling
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Metabolic status analyzed by the amount of metabolic products found in fecal, urine and serum samples
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Measured from single time point sampling
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KAURA2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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