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Food Allergy in ChildrenNCT07105865

The Role of NIchel and LTPs Sensitization in Functional Gastrointestinal Disorders: the NILT Study

An observational study of Food Allergy in Children, run by Federico II University at 1 site in Italy.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Non-specific lipid transfer proteins (nsLTPs) are currently recognized as the most prevalent cause of primary IgE-mediated food allergy in Mediterranean populations and constitute a leading trigger of anaphylactic reactions. Read more about this study

Who is it for?
Ages 4 to 65 years
Conditions the study is for
Food Allergy in Children
How many people
100 participants
Where
1 siteItaly
Study dates
1 Jul 2025to 1 Jul 2027
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 4 to 65 years
  • All sexes
  • Child, Adult, Older adult

Study population: 50 adults (>18 years) and 50 pediatric (4-17 years), of both sexes, belonging to the Adult Gastroenterology Programs and Pediatrics Section of Department of Translational Medical Sciences (University of Naples Federico II).

Who may be able to join

  • Age at least of 4 years
  • both sexes
  • history of functional dyspepsia (according to the Rome IV criteria, at least one symptom among the following - duration of symptoms greater than 4 days per month and for more than 2 consecutive months, feeling of post-prandial fullness, early satiety, pain and/or epigastric burning not associated with defecation - in the absence of organic disease) and irritable bowel syndrome (according to the Rome IV criteria, including all of the following criteria for at least 2 months prior to diagnosis - abdominal pain for at least 4 days per month associated with one/more of the following: change in EF, change in stool shape/appearance, if constipation is noticed, pain does not resolve with resolution of constipation - in the absence of organic disease).
  • written informed consent from the parents of the participants and the participants if over 6 years of age.

Who cannot join

  • Age < 4 years
  • Evidence of gastrointestinal pathology of organic nature (GERD, Helicobacter Pylori infection, eosinophilic diseases, celiac disease, chronic inflammatory bowel disease, chronic pancreatitis, cholelithiasis, neoplasia); motility disorder on a post-infectious basis; food intolerances (e.g. lactose), carbohydrate malabsorption, use of ASAs, NSAIDs; chronic systemic diseases (diabetes, amyloidosis, neuropathy) and autoimmune diseases; neuropsychiatric disorders; pregnancy.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Italy1 site, 1 recruiting
  • Department of Traslational Medical Science - University of Naples Federico II

    Naples, Naples, 80131

    Roberto Berni Canani, MD, PhD, 0817462680, berni@unina.it

    Recruiting

Other trials in Italy

About this study

Non-specific lipid transfer proteins (nsLTPs) are currently recognized as the most prevalent cause of primary IgE-mediated food allergy in Mediterranean populations and constitute a leading trigger of anaphylactic reactions. In Italy, the prevalence of LTP sensitization is estimated at 2-2.4% in adults and approximately 9% in children, with marked geographic variation. Specifically, higher prevalence rates are observed in central and southern regions and on the islands (21.3%-27.2%) compared to the northern regions (approximately 11%).

LTPs are ubiquitous panallergens, widely expressed throughout the plant kingdom. They represent the major allergens within the Rosaceae family in individuals not sensitized to birch pollen and have also been identified and characterized in numerous plant-derived foods, including nuts, legumes, rice, maize, beer, spelt, and wheat. The clinical spectrum of LTP hypersensitivity is highly heterogeneous. While a significant proportion of sensitized individuals remain asymptomatic, others may present with localized reactions such as contact urticaria or oral allergy syndrome (OAS). More severe cases may involve gastrointestinal symptoms (e.g., vomiting, epigastric discomfort, abdominal pain), cutaneous and respiratory manifestations, and systemic responses up to anaphylactic shock.

Read more

Nickel is a ubiquitous metal employed in a wide range of industrial applications and consumer products, including stainless steel, metal plating, various alloys, and inexpensive jewelry. It is also naturally present in both animal and plant-based food sources (e.g., cereals, cocoa, legumes, fresh fruits and nuts, fish). Nickel is the most common sensitizer in allergic contact dermatitis, affecting approximately 20% of the general population and around 10% of the pediatric population. Sensitization to nickel involves a delayed-type (Type IV) hypersensitivity reaction and is not IgE-mediated. Clinical manifestations range from localized allergic contact dermatitis to systemic involvement, referred to as systemic nickel allergy syndrome (SNAS), which is characterized predominantly by gastrointestinal symptoms, although respiratory and other systemic manifestations can also occur.

Gastrointestinal symptoms such as gastroesophageal reflux disease (GERD), functional dyspepsia, abdominal pain, and altered bowel habits, when not associated with overt allergic signs or underlying organic disease, are typically classified as functional gastrointestinal disorders (FGIDs). Several studies report that up to 40% of adult patients with FGIDs exhibit nickel sensitization; however, data in the pediatric population remain scarce.

Chelanik® is a dietary supplement designed to support individuals with nickel hypersensitivity. It contains bioactive components purported to exert immunomodulatory and anti-inflammatory effects. Nevertheless, in vitro human data directly demonstrating its activity on lymphocyte function are currently lacking.

This prospective, experimental, single-center study aims to determine the prevalence of sensitization to LTP and nickel among patients presenting with functional dyspepsia or irritable bowel syndrome (IBS), and to assess in vitro the potential immunomodulatory effects of Chelanik® on peripheral blood lymphocytes from individuals with nickel allergy.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Prevalence of nickel and LTP sensitization in patients with symptoms of functional dyspepsia and irritable bowel syndrome

    To evaluate the prevalence of nickel and LTP sensitization in patients with symptoms of functional dyspepsia (according to the Rome IV criteria, at least one symptom among the following for at least 4 days at the month and for at least 2 months before diagnosis - feeling of post-prandial fullness, satiety early epigastralgia or heartburn unrelated to defecation - in the absence of organic disease) and irritable bowel syndrome (according to Rome IV criteria, including all of the following for at least 2 months before diagnosis - abdominal pain for at least 4 days per month associated with one/more of the change in evacuation frequency, change in the shape/appearance of stools, if constipation is noticed pain does not resolve with the resolution of constipation - in the absence of organic disease).

    Measured: At baseline

Secondary outcomes (3)
  1. Diagnostic accuracy of the patch test with peach juice

    The atopy patch test is evaluated through visual inspection 48 hours after patch removal, with an optional second reading at 72 hours to detect delayed reactions.

    The reaction at the application site is assessed based on its intensity and classified according to a semi-quantitative scale:

    • +: erythema with infiltration
    • ++: erythema with a few papules
    • +++: erythema with numerous or widespread papules
    • ++++: erythema with vesicles.

    Measured: At baseline

  2. Evaluation of the potential immunomodulatory effect of Chelanik® on blood mononuclear cells: characterization and activation of CD4+ and CD8+ T populations

    Flow cytometric analysis

    For the analysis of phenotypes by multiparametric flow cytometry, the following will be used:

    Antibody panels:

    • T cell panel: anti-CD3, anti-CD4, anti-CD8, anti-HLA-DR (anti-CD4, anti-CD8, anti-HLA-DR (anti-CD4, anti-CD8, anti-HLA-DR (anti-CD4, anti-CD4, anti-CD4, anti-CD4, anti-CD4, anti-CD8, anti-HLA-DR (anti T lymphocytes), CD45RA (na.ve lymphocytes), CCR7 (memory T cells) and CD38 (activation).
    • Th1/Th2/Th17 panel: CD3, CD4, CD8, HLA-DR, CCR4 (Th2-associated marker), CCR6 (Th17), CXCR3 (Th1), and CD38 (activation).
    • Regulatory T cell panel: CD3, CD4, CCR4 (Treg migration), CD25 (activation) and CD127.

    Measured: At baseline

  3. Evaluation of the potential immunomodulatory effect of Chelanik® on blood mononuclear cells: cytokines production

    Cytokine assay by ELISA test Analysis of cytokine expression levels (IL-2, IL-5, IL-13, IL-4, IL-22, IFN-γ, IL-17, TNF-α, IL-10) will be. performed on both serum and supernatants of PBMCs cultures. The concentrations of the individual cytokines will be quantified by ELISA enzyme immunoassay, according to the protocols and recommendations provided by the manufacturer of the kit used.

    Measured: At baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Aug 2025
  2. Study start1 Jul 2025
  3. Primary completion1 Jul 2027 (estimated)
  4. Study completion1 Jul 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07105865
Sponsor's protocol ID
283/2025
Status last verified
Jul 2026
First submitted
16 Jul 2025
Last updated
1 Sep 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Food Allergy in Children, run by Federico II University at 1 site in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 1 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Prevalence of nickel and LTP sensitization in patients with symptoms of functional dyspepsia and irritable bowel syndrome (time frame: At baseline). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Sep 2026.

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