Genetic Study of Immunodeficiency: Search for New Genetic Causes for Primary Immunodeficiencies

Recruiting now

Conditions studied: Immunologic Deficiency Syndromes, Primary Immune Deficiency (PID)

In brief

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.

Key facts

Study ID

NCT02735824

Run by

University Children's Hospital, Zurich

People needed

500

Starts

2016-02-01

Expected to finish

2027-12-01

Last updated by the study team

2026-05-14

Who can join

Age: any. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients: Pediatric patients (in/outpatient or referred) with suspected or confirmed Inborn Errors of Immunity.
• Relatives: Healthy or affected biological relatives of enrolled patients.
• Controls: Healthy volunteers with no history of chronic immunological, inflammatory, or infectious disease.
• Consent: Ability to provide signed informed consent (or guardian consent).

Where it is running

• Division of Immunology — Zurich, Canton of Zurich, Switzerland (enrolling)

Full record on ClinicalTrials.gov

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