Feasibility Study of a New Immunoglobulin E (IgE) Assay Method
Recruiting now
Conditions studied: Allergy and Immunology
In brief
The main objective is to study the feasibility of a new specific IgE assay using a bioluminescence technique in a pediatric and adult allergic population. For this, we will collect blood, and urine during a blood test scheduled for the follow-up of the patient.
Key facts
- Study ID
- NCT04751760
- Run by
- University Hospital, Toulouse
- People needed
- 1376
- Starts
- 2021-04-20
- Expected to finish
- 2026-04-20
- Last updated by the study team
- 2026-03-19
Who can join
Age: 1 and older, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Males or females 6 months' old or older
- Sensitization or allergy towards a trophallergen, an aeroallergen, hymenoptera venom or drug proven by:
- positive skin test (s)
- and / or IgE specific (s)> 0.1 kUA / L
- and / or anamnesis in favor of an allergic reaction of mediated IgE
- Social coverage up to date
You may not qualify if…
- Children younger than 6 months'old
- Children's weight less than 10 kg
- Pregnant or breastfeeding women
- Patients with cystic fibrosis
- Patients with dysimmune or autoimmune pathology
- Anamnesis in favor of a delayed allergy or a contact allergy.
Where it is running
- University Hospital — Toulouse, France (enrolling)
- Larrey hospital — Toulouse, France (enrolling)
Full record on ClinicalTrials.gov
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