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Registry of Vaccine Responses in Immune Compromised Patients

Recruitingn/aAges any - anyAllLaure Pittet, MD-PhD
NCT06463119 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The aim of this project is to monitor, guide and document vaccination, vaccine responses, persistence of protection, vaccine efficacy and safety in immune compromised patients at various moment of their disease: right after the diagnosis, before the introduction of the immunosuppressive treatment, once the individual is under immunosuppressive treatment, or once immunosuppression is over.

Sign in to get the eligibility rules as simple questions to take to your doctor.

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Immune compromised patient or patient who will soon be immunocompromised 2. Informed consent as documented by signature Exclusion Criteria: 1. Individual/parental inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, known/suspected non-compliance, substance abuse, etc. 2. Plan to move out of the country or have prolong absence in the next 2 months
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What it tests

  • Collection of data in a registry
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Where

1 site
University Hospitals of Geneva
Geneva, Switzerland
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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