Bioelectrical Impedance Analysis of Not-celiac Wheat Sensitivity Patients
NCT ID: NCT01762566
Last Updated: 2014-09-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2012-01-31
2013-12-31
Brief Summary
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For the investigators' research, the investigators selected adult patients, both genders, affected with NCWS. Diagnostic criteria include: 1) symptoms disappearance on GFD, 2) testing negative for celiac disease \[anti-tTG and EMA, and with biopsy Marsh 0-1\] and wheat allergy \[serum specific IgE for wheat\], 3) positive response to a double-blind placebo-controlled challenge (DBPC) with wheat or placebo.
Patients will be recruited among subjects referring, as outpatients, to the Department of Internal Medicine, 'Giovanni Paolo II' Hospital of Sciacca (Agrigento), and of Internal Medicine of the University of Palermo, from January 2012 to October 2013. The investigators will include patients referring for functional dyspepsia and/or irritable bowel syndrome (IBS)-like symptoms. All recruited patients must report body's swelling immediately after wheat ingestion. In all recruited patients, NCWS diagnosis was posed during the previous years, according to the above mentioned criteria.
Patients, all on GFD for at least 30 days, will undergo to another DBPC with wheat or placebo (xylose), performed by administering capsules coded as A or B containing wheat or xylose, respectively. Capsules A or B will be administered once, and then, after 1 week of washout, patients received the other capsules, given once too. Before and 2 hours after every challenge, patients will undergo a complete medical examination (measurement of body weight, height, body mass index \[BMI\], waist circumference, diameter of thighs, legs, arms, and fingers), and we will perform bioelectrical impedance analysis and collect blood sampling, for identification of possible markers (bioelectrical, immunologic, hormonal, etc) that may help to demonstrate and explain mechanisms of examined symptom.
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Detailed Description
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As it is not known what cereals components determine the symptoms in the so called gluten sensitivity patients, we prefer to define this condition as "wheat sensitivity" instead of "gluten sensitivity".
Wheat sensitivity can cause both gastrointestinal and extra-intestinal symptoms; among the latter, the patients often reported body's swelling (hands', fingers', arms' , face's swelling).
This study has two major aims:
1. Evaluation of the effective dependence from the wheat ingestion of the clinical alterations presented by patients with diagnosed gluten sensitivity, with particular attention to abdominal bloating and body's swelling. The study will be done after a period of gluten-free diet (at least 30 days), using a double-blind placebo-controlled challenge with wheat or placebo (xylose), performed by administering capsules coded as A or B containing wheat or xylose, respectively. Capsules A or B will be administered once, and then, after 1 week of washout, the patients received the other capsules, given once too.
2. Before and 2 hours after every challenge, patients will undergo a complete medical examination, and The investigators will perform bioelectrical impedance analysis and collect blood sampling, for identification of possible markers that may be of help to demonstrate and explain the mechanisms of the examined symptom.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
QUADRUPLE
Study Groups
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wheat
wheat is administered blindly versus placebo in capsules once
wheat
wheat is administered blindly versus placebo in capsules once
xylose
placebo (xylose) will be administered blindly versus wheat in a capsule once
xylose
placebo (xylose) will be administered blindly versus wheat in capsules once
wheat
wheat is administered blindly versus placebo in capsules once
xylose
placebo (xylose) will be administered blindly versus wheat in a capsule once
Interventions
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wheat
wheat is administered blindly versus placebo in capsules once
xylose
placebo (xylose) will be administered blindly versus wheat in a capsule once
Eligibility Criteria
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Inclusion Criteria
* Patients testing negative for celiac disease (i.e. anti-tTG and EMA negative, and with biopsy Marsh 0-1) and wheat allergy (serum specific IgE for wheat negative)
* gluten sensitivity diagnosis confirmed with a double-blind placebo-controlled challenge with gluten or placebo
Exclusion Criteria
* Patients diagnosed with wheat allergy (positive serum specific IgE for wheat)
* Patients suffering from Diabetes Mellitus
* Patients with Inflammatory Bowel Diseases (Crohn's disease or ulcerative colitis)
* Patients with Helicobacter pylori infection and other gastrointestinal infection
* Pregnancy
18 Years
65 Years
ALL
No
Sponsors
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University of Palermo
OTHER
Responsible Party
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Pasquale Mansueto
MD
Principal Investigators
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Antonio Carroccio, PHD
Role: PRINCIPAL_INVESTIGATOR
Internal Medicine, Giovanni Paolo II Hospital of Sciacca (Agrigento) and University of Palermo, Palermo, Italy
Locations
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Internal Medicine, "Giovanni Paolo II" Hospital
Sciacca, Agrigento, Italy
Internal Medicine, University Hospital of Palermo
Palermo, Palermo, Italy
Countries
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Other Identifiers
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ACPM02
Identifier Type: -
Identifier Source: org_study_id
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