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Prospective Observational Trial of IAPA

Influenza-associated Pulmonary Aspergillosis (IAPA) in ICU Patients With Severe Influenza: Incidence and Host- and Pathogen Related Risk Factors

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04530799
Acronym
IAPAFLU
Enrollment
241
Registered
2020-08-28
Start date
2022-03-10
Completion date
2026-05-18
Last updated
2026-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Influenza With Pneumonia, Pulmonary Aspergillosis

Keywords

Influenza, Intensive Care Unit, Influenza-associated pulmonary aspergillose, Invasive Pulmonary Aspergillosis, Virus Diseases, Respiratory tract infections, Fungal Lung Diseases

Brief summary

A prospective multi-center observational study to assess the incidence of influenza-associated pulmonary aspergillosis (IAPA) in ICU patients and to identify host- and pathogen related risk factors for IAPA in EORTC negative ICU patients with severe influenza.

Detailed description

Invasive pulmonary aspergillosis was shown to be a complication of severe influenza infections in immunocompromised patients as well as in immunocompetent patients and is associated with a high mortality. Antifungal prophylaxis might prevent influenza-associated pulmonary aspergillosis (IAPA) and thus might improve the outcome in patients with severe influenza. However, clinical related risk factors should be identified to assess whether a patient will benefit from antifungal prophylaxis. This prospective multi-center observational study will assess the incidence of influenza-associated pulmonary aspergillosis (IAPA) in ICU patients in 12 ICUs in The Netherlands, Belgium and France over 4 influenza seasons. The secondary objective of this study is to identify host- and pathogen related risk factors for IAPA in EORTC negative ICU patients with severe influenza. Patients aged 18 or older admitted to the intensive care unit (ICU) during the inclusion period due severe influenza without classic risk factors defined by the EORTC will be included.

Interventions

OTHERIdentification of biomarkers for IAPA via patient sampling

Blood, BAL, microbiome

Sponsors

Radboud University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with a PCR-positive respiratory virus panel (RVP) result for influenza within 96 hours before or 48 hours after ICU admission. * Patients who require ICU admission for more than 24 hours for severe influenza. * Patients who have respiratory distress (respiratory rate \>= 25x/minute and paO2/fiO2 \< 300 with or without bilateral infiltrates) as the main reason for ICU admission. * Patients who do not have an EORTC host factor. * Patients who are at least 18 years of age.

Exclusion criteria

* Patients with age \< 18 years as extensive sampling is required * Expected survival on ICU admission ≤ 48h * Patients that are being treated actively with antifungal agents for invasive aspergillosis. * Patients or their legal representatives who did not sign the informed consent form

Design outcomes

Primary

MeasureTime frameDescription
The incidence of IAPA-infection at ICU dischargefrom date of admission in ICU assessed up to ICU discharge, approximately 21 daysThe diagnosis of IAPA will be made by the treating physician, according to a strict case definition.

Secondary

MeasureTime frameDescription
Time to IAPA diagnosisfrom date of admission in ICU assessed up to ICU discharge, approximately 21 daysThe diagnosis of IAPA will be made by the treating physician, according to a strict case definition.
Length of ICU stayfrom date of admission in ICU assessed up to ICU discharge, approximately 21 days
Length of hospital stayfrom date of admission in hospital assessed up to hospital discharge, approximately 30 days
ICU mortalityup to ICU discharge, approximately 21 days
Hospital mortalityfrom date of admission in hospital assessed up to hospital discharge, approximately 30 days
30-day mortality30 days
90-day mortality90 days

Countries

Belgium, France, Netherlands

Contacts

PRINCIPAL_INVESTIGATORJoost Wauters, MD, PhD

UZ Leuven

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 19, 2026