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Clinical Trials in Belgium / NCT07328178
Recruiting Observational

Analysis of the Role of IgE Proteoforms in Health and Disease

NCT07328178 · tracked via the Priya Life Science Belgium tracker
Sponsor
Phase
Observational
Started
2025-01-01
Last updated
2026-01-09

Condition(s) studied

AnaphylaxisMastocytosisX-linked AgammaglobulinaemiaVenom AllergyChronic Spontaneous Urticaria (CSU)Type I AllergyMedication AllergyHealthy ControlHereditary Alpha-Tryptasemia

Investigational drug(s) / intervention(s)

Blood sample collection

Blood sample collection: Blood sample collection

Study summary

The goal of this observational study is to evaluate the role of IgE proteoforms in healthy volunteers and in patients with type I allergy, patients with chronic spontaneous urticaria, patients with a recent history of anaphylaxis, patients with mastocytosis, patients with hereditary alpha tryptasemia, patients with X-linked agammaglobulinemia (XLA), and patients undergoing desensitization for venom or medication allergy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * CSU and type I allergic diseases (including anaphylaxis and desensitization), atopic dermatitis, mastocytosis, XLA and HaT (informed consent, age: any available adult subject, gender: any available subject, clinical phenotype and specific information about the allergy (e.g. severity, medication, medical history, laboratory testing) * Healthy controls (informed consent, age matched to the allergic patients, gender matched to the allergic patients, patient-reported symptoms related to allergy to aeroallergens, food, drugs, hymenoptera venom, CSU) Exclusion Criteria: * Absence of informed consent * Age \< 18 years old

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
UZ/KU Leuven Leuven Vlaams-Brabant Recruiting

More KU Leuven trials in Belgium

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07328178 on ClinicalTrials.gov ↗ ← All trials in Belgium