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Low Doses Corticosteroids as Adjuvant Therapy for the Treatment of Severe H1N1 Flu

Phase III Study of Hydrocortisone in Patients With Severe H1N1 Related Pneumonia

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01014364
Acronym
CORTIFLU
Enrollment
40
Registered
2009-11-17
Start date
2010-03-31
Completion date
2011-12-31
Last updated
2014-12-18

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

Conditions

Influenza in Humans, Pneumonia, Viral

Keywords

Acute lung injury, Acute respiratory distress syndrome, corticosteroids, inflammation

Brief summary

The H1N1 flu pandemic is one of the major infectious threat of the past half century. it is rapidly progressing worldwide and a substantial number of patients get severe H1N1 related pneumonia that requires mechanical ventilation and admission to the intensive care unit. The acute respiratory distress syndrome is associated with a substantial mortality and morbidity partly as a consequence of uncontrolled lung and systemic inflammation. many physicians are trying to counteract this pro-inflammatory storm by the use of corticosteroids albeit these drugs may cause super infection or metabolic disorders. Thus, there is a need for a randomized double blind, placebo controlled trial to define the benefit to risk ratio of corticosteroids in this patient.

Interventions

DRUGhydrocortisone

50mg intravenous bolus every 6 hours for one week, then every 12 hours for one week and then every 24 hours for one week

DRUGisotonic saline

intravenous bolus every 6 hours for one week, then every 12 hours for one week and then every 24 hours for one week

Sponsors

Assistance Publique - Hôpitaux de Paris
CollaboratorOTHER
University of Versailles
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

* age above 15 years old * admitted to intensive care unit * proven or strong suspicion of H1N1 Influenza infection * diffuse pneumonia (for less than 96 hours) * need for non invasive or invasive mechanical ventilation

Exclusion criteria

* pregnancy * an age of 15 or less * rapidly fatal underlying disease with a life expectancy of one month or less * more than 3 organ dysfunction upon admission * previous treatment with corticosteroids (ie prednisone 30 mg per day or more, or equivalent, for at least one month) * formal indication for corticosteroids (eg Addison disease, status asthmaticus) * already on corticosteroids for 2 days or more in the management of the current episode * acute lung injury not related to viral pneumonia * presence of H1N1 related acute myocarditis or encephalitis * receiving antiviral treatment for more than 5 days

Design outcomes

Primary

MeasureTime frame
in hospital all cause moralityhospital discharge up to 90 days

Secondary

MeasureTime frame
90 day all cause mortality90 day
6 month all cause mortality180 days
mechanical ventilation free dayshospital discharge up to 90 days
28 day mortality28 day
proportion of patients with secondary infectionshospital discharge up to 90 days
proportion of patients who require ECMOhospital discharge up to 90 days
respiratory function and health status180 days
intensive care unit free dayshospital discharge up to 90 days

Countries

France

Outcome results

None listed

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