Registry of Vaccine Responses in Immune Compromised Patients
Recruiting
Observational Study
Immunosuppression
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
Ready to participate?
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At a Glance
Sex
Any
Study type
Observational
Participants needed
300 (estimated)
Sponsor
Laure Pittet, MD-PhD · Other
Who this trial is looking for
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
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.
Trial Locations
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City
State
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Status
Eligibility Criteria
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/…
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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