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Completed
NCT04486885
European Study of Cerebral Aspergillosis Treated With Isavuconazole
Conditions: Cerebral Aspergillosis, Invasive Aspergillosis
Sex: All
Healthy volunteers: No
Enrollment: 41
Sponsor: Imagine Institute
Location: Hôpital Necker-Enfants Malades Paris
Summary
Study clinical context Cerebral aspergillosis (CA) is a rare location of invasive aspergillosis (IA), associated with a high morbidity and mortality. Since 2002, voriconazole is the recommended first line treatment of invasive aspergillosis. More recently, isavuconazole appeared to be not less effective than voriconazole in the treatment of filamentous IFI, with a better tolerance profile.
The investigators aim to evaluate better the efficacy and the safety of isavuconazole in the treatment of cerebral aspergillosis by a descriptive, multicentric, international retrospective cohort study.
Eligibility Criteria
Inclusion Criteria:
* Proven or probable cerebral aspergillosis according to the EORTC criteria modified by adding diabetes in the host criteria
* In child or adult
* Treated by isavuconazole at least 7 days
* Diagnosed between March 2017 and June 2020
Exclusion Criteria:
* Possible cerebral aspergillosis
* isavuconazole treatment for less than 7 days
Source: ClinicalTrials.gov (NCT04486885). StuddyBuddy aggregates publicly available trial information.