Actively Recruiting

All Genders
ID05210543

Acquisition and Long-term Observation of Patients With Severe Allergic Reactions

Led by Charite University, Berlin, Germany · Updated on 2024-08-21

20000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Acquisition and Long-term Observation of Patients With Severe Allergic Reactions

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Experienced an anaphylactic reaction within the past 12 months
Not Eligible

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

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

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.

Trial Site Locations

Total: 1 location

1

Charité - Universitätsmedizin Berlin

Berlin, Germany, 10117

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Research Team

M

Margitta Worm, Prof.

S

Sabine Dölle-Bierke, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial