Oat Products in the Treatment of Coeliac Disease in Children

March 17, 2015 updated by: Heinz Italia SpA

Multicentre Clinical Trial on Oat Products in the Treatment of Coeliac Disease in Children

In many Northern European countries oat-based products have been used in the dieto-therapy of coeliac disease for many years.

The purpose of this study is to evaluate clinical tolerance and liking of gluten-free products containing oatmeal from a specific oat variety (not contaminated with gluten) in a sample of Italian celiac patients in pediatric age.

Study Overview

Status

Unknown

Intervention / Treatment

Detailed Description

Several clinical trials have demonstrated that most celiac patients, both of pediatric and of adult age, can take medium-high quantity of oat (50-100 g/day), without any negative clinical effects.

In a small number of cases intestinal dyspeptic disorders, especially meteorism, can be observed, particularly during the first weeks of oat intake. They are generally without clinical significance because they are a consequence of the increased fibre intake.

There are only few cases of "true" oats intolerance. The addition of oat improves the nutritional quality of the gluten-free diet, particularly due to the increased intake of fibre and some oligoelements (iron, zinc, tiamin, pholates) and expands the spectrum of food choices.

In many Northern European countries oat-based products have been used in the dieto-therapy of coeliac disease for many years.

For the oat-based product to be considered suitable in the dieto-therapy of coeliac disease, the absence of gluten contamination and possibly the origin from a variety of oat which is without traces of gluten cross-reactive peptides must be guaranteed.

The purpose of this study is to evaluate clinical tolerance and liking of gluten-free products containing oatmeal from a specific oat variety (not contaminated with gluten) in a sample of Italian celiac patients in pediatric age.

Study Type

Interventional

Enrollment (Anticipated)

300

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Ancona, Italy, 60123
        • Università Politecnica delle Marche, Clinica Pediatrica
      • Bari, Italy, 70124
        • Ospedale Policlinico Consorziale, Clinica Pediatrica "B.Trambusti"
      • Bolzano, Italy, 39100
        • Ospedale Centrale, Divisione di Pediatria
      • Monza, Italy, 20052
        • Azienda Ospedaliera "San Gerardo", Clinica Pediatrica
      • Roma, Italy, 00161
        • Azienda Policlinico "Umberto I" - Dip. di Pediatria - UOC di Gastroenterologia ed Epatologia Pediatrica
    • CT
      • Catania, CT, Italy, 95124
        • Azienda Ospedaliero-Universitaria "Policlinico Vittorio Emanuele"
    • Salerno
      • Cava de' Tirreni, Salerno, Italy, 84013
        • Ospedale Civile "S. Maria Incoronata dell'Olmo", Divisione di Pediatria

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

4 years to 14 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria: the study will include patients aged between 4 and 14, under treatment with a gluten-free diet for coeliac disease (bioptic diagnosis) for at least two years.

Exclusion Criteria:

diagnosis not confirmed by intestinal biopsy, cases with little adherence to the treatment (anti-tTG positive at basal evaluation), cases of potential coeliac disease (completely normal mucous membrane), cases with an associated sieric IgA deficit, cases with associated diseases (es. diabetes type 1).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: A/B
This is a cross-over design, i.e. each patient is treated with either oat or control products in different times.
Gluten-free bakery products containing oatmeal.
Other Names:
  • BiAglut

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Clinical safety through serological markers of coeliac disease and intestinal wall integrity, clinical and bioumoral parameters of nutrition status, frequency and clinical type of dyspeptic disorders or other adverse reactions.
Time Frame: Controls at recruiting, after 3, 6, 9, 12, 15 months from the beginning of the study.
Controls at recruiting, after 3, 6, 9, 12, 15 months from the beginning of the study.

Secondary Outcome Measures

Outcome Measure
Time Frame
Liking of gluten-free products containing oatmeal is evaluated through a product liking questionnaire.
Time Frame: Product liking questionnaire after 6 months and 15 months from the beginning of the study.
Product liking questionnaire after 6 months and 15 months from the beginning of the study.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Carlo Catassi, Prof., Università Politecnica delle Marche - Clinica Pediatrica - Ancona
  • Principal Investigator: Ruggiero Francavilla, Dr., Ospedale Policlinico Consorziale, Clinica Pediatrica "B.Trambusti" - Bari
  • Principal Investigator: Klaus Pittschieler, Prof., Ospedale Centrale di Bolzano
  • Principal Investigator: Basilio Malamisura, Prof., Ospedale Civile "S. Maria Incoronata dell'Olmo" - Cava de' Tirreni (SA)
  • Principal Investigator: Roberto Panceri, Dr., Azienda Ospedaliera "San Gerardo" - Monza
  • Principal Investigator: Maria Barbato, Prof., Azienda Policlinico Umberto I, Roma
  • Principal Investigator: Mario La Rosa, Prof., Azienda Ospedaliero-Universitaria Policlinico Vittorio Emanuele, Catania

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2009

Primary Completion (Actual)

July 1, 2014

Study Completion (Anticipated)

October 1, 2015

Study Registration Dates

First Submitted

December 12, 2008

First Submitted That Met QC Criteria

December 12, 2008

First Posted (Estimate)

December 15, 2008

Study Record Updates

Last Update Posted (Estimate)

March 18, 2015

Last Update Submitted That Met QC Criteria

March 17, 2015

Last Verified

March 1, 2015

More Information

Terms related to this study

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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