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.
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
- Recruiting
Department of Traslational Medical Science - University of Naples Federico II
Naples, Naples, 80131
Roberto Berni Canani, MD, PhD, 0817462680, berni@unina.it
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.
- Conditions
- Food Allergy in Children
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
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
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
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.
- First posted6 Aug 2025
- Study start1 Jul 2025
- Primary completion1 Jul 2027 (estimated)
- Study completion1 Jul 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Food Allergy in ChildrenStudies of the same condition, open and under way.
- More trials run by Federico II UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Federico II University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Roberto Berni Canani, MD, PhD, Federico II University
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
Study at a glance
From the registry record, last updated by the sponsor on 1 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Role of NIchel and LTPs Sensitization in Functional Gastrointestinal Disorders: the NILT Study
- ClinicalTrials.gov ID
- NCT07105865
- Acronym / sponsor ID
- 283/2025
- Conditions
- Food Allergy in Children
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 100 participants (estimated)
- Lead sponsor
- Federico II UniversityUniversity, hospital or other
- Study start
- 1 Jul 2025 (actual)
- Primary completion
- 1 Jul 2027 (estimated)
- Study completion
- 1 Jul 2027 (estimated)
- First posted
- 6 Aug 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 4 to 65 years
- Sex
- All
- Age groups
- 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).
Key inclusion criteria (4 listed)
- 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.
Key exclusion criteria (2 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Prevalence of nickel and LTP sensitization in patients with symptoms of functional dyspepsia and irritable bowel syndrome
Time frame: At baseline
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).
3 secondary outcomes
Diagnostic accuracy of the patch test with peach juice
Time frame: At baseline
Evaluation of the potential immunomodulatory effect of Chelanik® on blood mononuclear cells: characterization and activation of CD4+ and CD8+ T populations
Time frame: At baseline
Evaluation of the potential immunomodulatory effect of Chelanik® on blood mononuclear cells: cytokines production
Time frame: At baseline
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Sep 2026.
Related trials for Food Allergy in Children
Recruiting
Evaluation of the Tolerance of a New Formula Based on Hydrolyzed Rice Proteins in Children With Cow's Milk Allergy
IgE-Mediated Cow Milk Allergy
Not yet recruiting
Rapid Escalation Oral Immunotherapy to Achieve Remission in Children With Cashew Allergy
Food Allergy in Children
Active, not recruitingPhase 2
A Safety and Efficacy Study of PVX108 in Children and Adolescents With Peanut Allergy
Peanut Allergy, Peanut Hypersensitivity
Not yet recruiting
Immunotherapy for Curing Toddlers With Severe Food Allergy - a Paradigm Shift From Passive to Active Treatment With Multi-allergen Oral Immunotherapy
Food Allergy in Children
Active, not recruiting
Slow Multiallergen Oral Immunotherapy in Young Children
Food Allergy, Oral Immunotherapy for Food Allergy
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Department of Traslational Medical Science - University of Naples Federico II
Naples, Italy
1 site in 1 country: see every site and its status.
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.