Skip to content

Severe Influenza Cohort

Identification, in Patients Admitted to Intensive Care for Severe Influenza Respiratory Infection, of a Predictive Biomarker of Respiratory Distress

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02392858
Acronym
ANTIGRIPPE
Enrollment
227
Registered
2015-03-19
Start date
2015-01-16
Completion date
2019-01-31
Last updated
2025-12-04

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

Conditions

Influenza, Severe Respiratory Infection

Brief summary

Influenza is a major cause of morbidity and mortality. The investigators first goal is to evaluate soluble HLA-G5 isoform serum level as a potential marker of greater risk of death from Influenza respiratory illness in adult and pediatric patients hospitalized in reanimation. Secondly, the investigators collected respiratory samples in order to study the transcriptomic profiles of influenza-infected patients with severe symptoms.

Interventions

OTHERinfluenza cohort

Influenza is a major cause of morbidity and mortality. The investigators' first goal is to evaluate soluble HLA-G5 isoform serum level as a potential marker of greater risk of death from Influenza respiratory illness in adult and pediatric patients hospitalized in reanimation. Secondly, the investigators collected respiratory samples in order to study the transcriptomic profiles of influenza-infected patients with severe symptoms.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Months to 99 Years
Healthy volunteers
No

Inclusion criteria

* Patient (Adult or Pediatric) * Hospitalized in reanimation * With a laboratory confirmed Influenza * That agree to take part in the study * Affiliated to National Health Insurance For ancillary group : * Adult at least 60 years old * Presenting at hospital for a blood test

Exclusion criteria

* non willing to participate * Influenza infection with no respiratory symptoms * pregnancy For ancillary group : * Presence of immunodepression defined by: * Cancer, or cancer cured for less than 2 years * Corticosteroids, Methotrexate (MTX), anti Tumor Necrosis Factor (TNF), anti-CD20 * Infection in progress (fever)

Design outcomes

Primary

MeasureTime frameDescription
Change in ratio of the partial pressure of oxygen in arterial blood (PaO2) to the inspired oxygen fraction (FiO2), from admission at 7 days post-admissionThe first, third, fifth and seventh day of hospitalization in reanimationdecreased arterial PaO2/FiO2 ratio ≤ 100 mmHg (≤ 13.3 kPa)

Secondary

MeasureTime frameDescription
All cause mortality90 days after hospitalization
Extracorporeal membrane oxygenation requirement90 days after hospitalization
SOFA score (Adult) PELOD (Pediatric)The first, third, fifth and seventh day of hospitalization in reanimationElevated Score is considered as an evidence of clinical gravity

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026