ClinicalTrials.gg
Status unknownNCT05826405CAJESITOUpdated Apr 24, 2023

Efficacy and Safety of Oral Cashew Nut Immunotherapy in Children (CAJESITO)

An observational study in Allergy;Food and Allergy, Nut, sponsored by Central Hospital, Nancy, France. Status unknown. Open to participants aged 0 Years to 18 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-04-24.

Primary conditionNut HypersensitivityRegistry: Food HypersensitivityReclassifiedWhy we changed it
Registry
Food Hypersensitivity — the first condition term the registry derived for this study.
ClinicalTrials.gg
Nut Hypersensitivity
Why
  1. The study's listed conditions name Nut Hypersensitivity, a narrower term within Food Hypersensitivity.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Central Hospital, Nancy, France · Observational

The sponsor has not verified this record recently (last verified Apr 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
40
Ages
0 Years to 18 Years
Sex
All
01

Study summary

The objectives of the CAJESITO study are (i) to assess the tolerance of oral cashew nut immunotherapy, by describing the frequency and severity of allergic reactions during oral cashew nut immunotherapy and (ii )to assess the risk factors for severe allergic reactions during oral cashew nut immunotherapy (predictive factors, associated factors.

02

Conditions studied

  • Allergy;Food
  • Allergy, Nut

Browse trials for

Keywords

  • allergy
  • food allergy
  • cashew nut allergy
  • oral immunotherapy
  • pistachio allergy
03

In context

Nut Hypersensitivity Reclassified

33 studies on the registry are indexed under Nut Hypersensitivity; 9 are open to participants now.

This study's planned enrollment of 40 is below the median of 240 across 11 observational studies indexed under Nut Hypersensitivity.

Browse Nut Hypersensitivity studies →

Lead sponsor

Central Hospital, Nancy, France is the lead sponsor of 798 studies on the registry; 186 are open to participants now.

Compared within Nut Hypersensitivity, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Food Hypersensitivity. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
0 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

All patients from 0 to 18 years old followed in allergology at the University Hospital of Nancy benefiting from oral immunotherapy with cashew nuts for at least 18 months as of 02/28/2023

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients under the age of 18 with a proven allergy to cashew nuts and followed in the pediatric allergology unit of the University Hospital of Nancy.
  • Patients who have received oral cashew nut immunotherapy for at least 18 months as of 02/28/2023

Exclusion criteria

Exclusion Criteria:

  • Patients who have received oral cashew nut immunotherapy for less than 18 months.
  • Patients lost to follow-up for more than 3 years, i.e. last consultation dating from 2020 or earlier
05

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
40 participants (estimated)
Patient registry
No

Groups and cohorts

  • Cashew Nut allergic

    Other: No intervention

Interventions

  • OtherNo intervention

    No intervention, it's an observational study

06

What researchers measure

Primary outcomes

  1. Number of allergic reaction

    Time frame: during 6 months

Secondary outcomes

  1. Predictive factor of good tolerance

    age at onset

    Time frame: during 6 months

  2. antibody variation

    Modification of level of specific IgE and IGg4 with cashew nuts

    Time frame: during 6 months

  3. sustained unresponsiveness

    Tolerance of 1, 2, 4, 8g in isolated doses and 15g in total cumulative dose of cashew nuts during an oral challenge test with cashew nuts 3 months after stopping the daily consumption of 2g of cashew nuts

    Time frame: 9 months

  4. oral tolerance of pistachio

    Tolerance of 1, 2, 4, 8g in isolated doses and 15g in total cumulative dose of pistachio during an oral provocation test with pistachio 3 months after stopping the daily consumption of 2g of cashew nuts

    Time frame: 6 months

  5. Predictive factor of good tolerance

    antecedent of severe allergic reaction

    Time frame: 6 months

  6. Predictive factor of good tolerance

    initial reactogenic threshold

    Time frame: 6 months

  7. Predictive factor of good tolerance

    presence atopy (asthma, food allergy or atopic dermatitis)

    Time frame: 6 months

  8. Predictive factor of good tolerance

    initial specific IgE and Ana o3 levels

    Time frame: 6 months

07

Study locations

No study locations are listed for this record.

08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for May 2023; primary completion for May 2023, 0 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 7, 2023
First posted
Apr 24, 2023
StartEst.
May 10, 2023
Primary completionEst.
May 10, 2023
CompletionEst.
May 10, 2023
Last update
Apr 24, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 24, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05826405
Responsible party
Amandine DIVARET-CHAUVEAU (Principal investigator, Central Hospital, Nancy, France) — Principal investigator
First posted
Apr 24, 2023
Start date
May 10, 2023 (estimated)
Primary completion
May 10, 2023 (estimated)
Completion
May 10, 2023 (estimated)
Last update
Apr 24, 2023

Study contacts

Amandine AD DIVARET-CHAUVEAU, MCU PH
Contact
a.chauveau@chru-nancy.fr
+3383153695

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2023. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion