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Clinical Trial Summary

Severe infections in pediatric intensive care unit are not uncommon. Historically, the diagnosis of hereditary (primary) immune deficiency required a combination of recurrent clinical signs and biological stigmas. This paradigm is currently being questioned, and grows the hypothesis of a potential underlying genetic susceptibility in any severe infection. To date, the proportion of severe infections explained by an underlying immune deficiency is unknown. The aim of this prospective study is to assess the incidence of primary immune deficiencies in children with severe infection, regardless of their etiology.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04990908
Study type Observational
Source University Hospital, Montpellier
Contact Eric JEZIORSKI
Phone 04 67 33 57 98
Email e-jeziorski@chu-montpellier.fr
Status Recruiting
Phase
Start date September 4, 2023
Completion date September 4, 2026

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