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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04232956
Other study ID # ASPERGIGRIPP (29BRC18.0069)
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 27, 2018
Est. completion date November 5, 2018

Study information

Verified date January 2020
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Invasive pulmonary aspergillosis (IPA) has been reported in critically ill patients with influenza infection with a highly variable incidence between 1 to 21%. Studies investigating IPA in critically ill patients with influenza infection suffer limitations in their methods. It remains unknown whether patients with influenza are more at risk of IPA than other patients hospitalized in intensive care unit and whether patients with influenza who develop IPA have specific risk factors for this infection.

Our study aims to determine the incidence of IPA in a large multicenter cohort and to identify risk factors for IPA in these patients.


Recruitment information / eligibility

Status Completed
Enrollment 478
Est. completion date November 5, 2018
Est. primary completion date November 5, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Infection with influenza A or B

- Admission to one of the participating sites

Exclusion Criteria:

- age < 18

- patients with invasive pulmonary aspergillosis prior to intensive care admission

- consent withdraw

Study Design


Locations

Country Name City State
France CHRU de Brest Brest
France CHR Morlaix
France CHU de NANTES Nantes
France CHU de Rennes Rennes

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Invasive Pulmonary Aspergillosis incidence of invasive pulmonary aspergillosis up to 100 days
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