Allergen immunotherapy-induced anaphylaxis: Data from the European Anaphylaxis Registry.
Meslina Almaci, Regina Treudler, Maria Breiding...
https://pubmed.ncbi.nlm.nih.gov/39993472Actively Recruiting
Led by Charite University, Berlin, Germany · Updated on 2024-08-21
20000
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are gathering detailed, standardized information about patients who have experienced anaphylactic reactions to better understand the symptoms, triggers, and management of these severe allergic responses. The study aims to improve diagnosis and long-term care for people affected by anaphylaxis by analyzing data collected over time. This research also explores genetic and biomarker factors that may influence the risk and severity of these reactions. Participants who have had an anaphylactic reaction are observed without receiving any specific treatment through the study. Blood sampling is optional but encouraged, as it helps identify sensitization profiles and possible biological mechanisms behind anaphylaxis. The study collects data over a long period, focusing on risk factors, use of adrenaline, country-specific management differences, and genetic and epigenetic markers related to anaphylaxis. Throughout the study, participants provide information and may undergo optional blood tests to help researchers track changes and outcomes related to their allergic reactions. The primary outcome measures include assessing risk factors over 10 years, along with secondary outcomes such as adrenaline use, biomarker validation, and epigenetic studies. This long-term observation helps enhance understanding of anaphylaxis and guides better prevention and treatment strategies for affected individuals.
CONDITIONS
Acquisition and Long-term Observation of Patients With Severe Allergic Reactions
You may qualify if you...
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 10 years
Participants who experienced an anaphylactic reaction are observed over time to better understand risk factors, biomarkers, and prognosis related to severe allergic reactions.
Total: 1 location
1
Charité - Universitätsmedizin Berlin
Berlin, Germany, 10117
Actively Recruiting
M
Margitta Worm, Prof.
S
Sabine Dölle-Bierke, PhD
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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Meslina Almaci, Regina Treudler, Maria Breiding...
https://pubmed.ncbi.nlm.nih.gov/39993472