Trials / Completed
CompletedNCT04172610
Prevalence of Influenza RelAted Invasive Aspergillosis
The Prevalence of Influenza Related Invasive Aspergillosis in Swedish Intensive Care Units
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 55 (actual)
- Sponsor
- Karolinska University Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a multicenter study with the aim to determine the prevalence of influenza-related invasive pulmonary aspergillosis in Swedish intensive care units and to assess the clinical impact of and risk factors for influenza-related invasive pulmonary aspergillosis
Detailed description
This is a multicenter prospective observational study conducted at 12 intensive care units (ICU) in Sweden. All patients \>18 years of age with a Polymerase Chain Reaction (PCR)-verified influenza A or B diagnosed up to 7 days before admission to the ICU or during ICU care, will be included in the study. A new clinical routine has been implemented at the study centers: During the ICU stay screening with Beta-D-glucan and Galactomannan in blood/serum will be performed twice weekly and a respiratory sample will be retrieved for fungal culture and microscopy once weekly. All results from collected samples will be available to the patient's attending physicians. Clinical and microbiological data will be collected, and the diagnosis of invasive aspergillosis will be made using predefined diagnostic criteria. Objectives: 1. To determine the prevalence of influenza-related invasive pulmonary aspergillosis in Swedish intensive care units 2. To assess the clinical impact of and risk factors for influenza-related invasive pulmonary aspergillosis
Conditions
Timeline
- Start date
- 2019-12-02
- Primary completion
- 2023-04-14
- Completion
- 2023-04-14
- First posted
- 2019-11-21
- Last updated
- 2023-07-06
Locations
12 sites across 1 country: Sweden
Source: ClinicalTrials.gov record NCT04172610. Inclusion in this directory is not an endorsement.