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Human recombinant interferon gamma in the treatment of ventilator-acquired pneumonia in ICU patients. IGNORANT study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-502229-16-00
Acronym
69HCL22_0851
Enrollment
132
Registered
2023-04-11
Start date
2023-06-19
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Ventilator acquired pneumonia

Brief summary

mechanical ventilation-free days (VFD) from extubation through D28. A beneficial effect of using recombinant human interferon gamma-1b would be a statistically significant increase in VFD in patients receiving study drug in this setting compared to the group receiving placebo.

Detailed description

All-cause mortality in intensive care at D28, Bacteriological samples become negative, The occurrence of another episode of VAP before extubation, length of stay in intensive care unit, length of stay at hospital, The evolution of monocytic HLA-DR kinetics, the evolution of leukocytes kinetics, Assessment of the economic efficiency of IFN-γ administration

Interventions

DRUG9 %
DRUGsolution injectable
DRUG1 mg)

Sponsors

Hospices Civils De Lyon
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
mechanical ventilation-free days (VFD) from extubation through D28. A beneficial effect of using recombinant human interferon gamma-1b would be a statistically significant increase in VFD in patients receiving study drug in this setting compared to the group receiving placebo.

Secondary

MeasureTime frame
All-cause mortality in intensive care at D28, Bacteriological samples become negative, The occurrence of another episode of VAP before extubation, length of stay in intensive care unit, length of stay at hospital, The evolution of monocytic HLA-DR kinetics, the evolution of leukocytes kinetics, Assessment of the economic efficiency of IFN-γ administration

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026