Diagnostic Significance of Positive EmA Antibodies in the Duodenal Culture Medium of Not-Celiac Wheat Sensitivity (NCWS) (NCWS)
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ClinicalTrials.gov Identifier: NCT02203201 |
Recruitment Status :
Completed
First Posted : July 29, 2014
Last Update Posted : October 8, 2020
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Condition or disease |
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Not-celiac Gluten Sensitivity |

Study Type : | Observational |
Actual Enrollment : | 50 participants |
Observational Model: | Case-Control |
Time Perspective: | Prospective |
Official Title: | Diagnostic Significance of Positive Anti-endomysium Antibodies in the Culture Medium of the Intestinal Biopsies in Not-Celiac Wheat Sensitivity (NCWS) |
Actual Study Start Date : | January 1, 2014 |
Actual Primary Completion Date : | October 1, 2016 |
Actual Study Completion Date : | June 1, 2020 |

Group/Cohort |
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Study group
NCWS patients who had showed a negative celiac disease serology and a Marsh 0-1 duodenal histology, but who had displayed a positive EmA assay in the culture medium of the duodenal biopsies (EmA-biopsy).
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Control group
NCWS patients with negative EmA-biopsy.
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- Changes in the intestinal histology of NCWS patients who tested positives for EmAs in the culture medium of the intestinal biopsies, at the time of the first evaluation. [ Time Frame: At baseline and after at least one year since the initial NCWS diagnosis was posed. ]
Intestinal histology re-evaluation after at least one year since the initial NCWS diagnosis was posed. Marsh classification will be adopted: change from baseline (1st evaluation) to 2nd evaluation.
The above parameter will be evaluated taking into account whether the patients adhered or not to a wheat-free diet.
- Serum anti-tTG antibodies evaluation. [ Time Frame: At baseline and after at least one year since the initial NCWS diagnosis was posed. ]Evaluation of changes in serum levels of anti-tTG antibodies after at least one year since the initial NCWS diagnosis was posed.
- Serum DPG antibodies evaluation. [ Time Frame: At baseline and after at least one year since the initial NCWS diagnosis was posed. ]Evaluation of changes in serum levels of DPG antibodies after at least one year since the initial NCWS diagnosis was posed.
- Serum AGA evaluation. [ Time Frame: At baseline and after at least one year since the initial NCWS diagnosis was posed. ]Evaluation of changes in serum levels of AGA after at least one year since the initial NCWS diagnosis was posed.
- Adherence to a wheat-free diet [ Time Frame: At baseline and after at least one year since the initial NCWS diagnosis was posed. ]Degree of adherence to a wheat-free diet since the initial diagnosis of NCWS was posed.
- Symptoms/signs evaluation. [ Time Frame: At baseline and after at least one year since the initial NCWS diagnosis was posed. ]The evaluation of changes in symptoms/signs will be made according to the score calculated on the basis of the Visual Analogue Scale since the initial diagnosis of NCWS was posed.

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Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Inclusion Criteria:
- Adult patients, both genders, with age between 18-65 years, that has been previously diagnosed as NCWS, according to a DBPC method
- Patients testing negative for celiac disease ( anti-tTG and EMA negative, and with biopsy Marsh 0-1) and wheat allergy (serum specific igE for wheat negative)
- Patients showed positive EmAs in the culture medium of the duodenal biopsies
Exclusion Criteria:
- Subjects diagnosed with celiac disease (positive anti-tTG and/or EMA, and positive histology, with Marsh 2 or above)
- Subjects diagnosed with wheat allergy (positive serum specific IgE for wheat)
- Subjects with Type 1 Diabetes
- Subjects with Inflammatory Bowel Diseases (Crohn's disease or ulcerative colitis)
- Subjects with Helicobacter pylori infection and other gastrointestinal infection
- Pregnancy

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02203201
Italy | |
Department of Internal Medicine, Giovanni Paolo II Hospital of Sciacca | |
Sciacca, Agrigento, Italy, 92019 | |
Department of Internal Medicine, University Hospital of Palermo | |
Palermo, Italy, 90129 |
Study Director: | Antonio Carroccio, MD, PhD | University of Palermo | |
Principal Investigator: | Pasquale Mansueto, MD | University of Palermo |
Responsible Party: | Pasquale Mansueto, Researcher, University of Palermo |
ClinicalTrials.gov Identifier: | NCT02203201 |
Other Study ID Numbers: |
ACPM04 |
First Posted: | July 29, 2014 Key Record Dates |
Last Update Posted: | October 8, 2020 |
Last Verified: | October 2020 |
Not-celiac gluten sensitivity Celiac Disease Gluten-free diet EMA assay Duodenal culture medium |
Celiac Disease Hypersensitivity Immune System Diseases Malabsorption Syndromes |
Intestinal Diseases Gastrointestinal Diseases Digestive System Diseases Metabolic Diseases |