Actively Recruiting
Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies
Led by University Children's Hospital, Zurich · Updated on 2026-05-14
500
Participants Needed
1
Research Sites
617 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Individuals with suspected primary immunodeficiency will be studied and the results compared with healthy controls. Primary immunodeficiency may manifest as recurrent, severe or unusual infections as well as signs and symptoms of immune dysregulation such as autoimmunity or lymphoproliferation.
CONDITIONS
Official Title
Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pediatric patients (inpatient or outpatient or referred) with suspected or confirmed Inborn Errors of Immunity
- Healthy or affected biological relatives of enrolled patients
- Healthy volunteers with no history of chronic immunological, inflammatory, or infectious disease
- Ability to provide signed informed consent or guardian consent
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
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Division of Immunology
Zurich, Canton of Zurich, Switzerland, 8008
Actively Recruiting
Research Team
J
Jana M Pachlopnik Schmid, MD PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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