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Influenza Associated Aspergillosis In-depth Investigation (PIAS)

U

Universitaire Ziekenhuizen KU Leuven

Status

Enrolling

Conditions

Influenza With Pneumonia
Invasive Pulmonary Aspergillosis

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

This trial is aimed to study the immunological and pathological characteristics of influenza versus non-influenza severe community-acquired pneumonia patients in ICU.

Full description

This trial is aimed to study the immunological and pathological characteristics of influenza versus non-influenza severe community-acquired pneumonia patients in ICU, and correlate findings with occurrence of secondary invasive pulmonary aspergillosis infection.

All consecutive patients aged 18 or older admitted to ICU during the inclusion period with respiratory distress due to influenza positive/negative community acquired pneumonia (CAP) will be included.

Enrollment

45 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients older than 18 years, admitted to ICU with respiratory distress with microbiologically confirmed diagnosis of influenza (for inclusion in the influenza group)
  • All patients older than 18 years, admitted to ICU for respiratory distress due to community- acquired pneumonia , with a microbiologically confirmed absence of influenza (for inclusion in the control group)

Exclusion criteria

  • Age < 18 years old
  • Pregnant women
  • No informed consent

Trial design

45 participants in 2 patient groups

Influenza positive CAPIV
Description:
All consecutive patients older than 18 years, admitted to the ICU with respiratory distress with microbiologically confirmed diagnosis of influenza
Influenza negative CAPIV
Description:
All consecutive patients older than 18 years, admitted to the ICU for respiratory distress due to community-acquired pneumonia (CAP) and with a microbiologically confirmed absence of influenza

Trial contacts and locations

1

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Central trial contact

Joost Wauters, PhD; Lore Vanderbeke, MD

Data sourced from clinicaltrials.gov

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