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

Sponsor
University of Versailles (Other)
Overall Status
Terminated
CT.gov ID
NCT01014364
Collaborator
Assistance Publique - Hôpitaux de Paris (Other)
40
1
2
21
1.9

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Actual Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Phase III Study of Hydrocortisone in Patients With Severe H1N1 Related Pneumonia
Study Start Date :
Mar 1, 2010
Actual Primary Completion Date :
Jun 1, 2011
Actual Study Completion Date :
Dec 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Experimental: Corticosteroids

Hydrocortisone

Drug: hydrocortisone
50mg intravenous bolus every 6 hours for one week, then every 12 hours for one week and then every 24 hours for one week
Other Names:
  • hydrocortisone acetate
  • Placebo Comparator: Control

    isotonic saline

    Drug: isotonic saline
    intravenous bolus every 6 hours for one week, then every 12 hours for one week and then every 24 hours for one week
    Other Names:
  • normal saline
  • Outcome Measures

    Primary Outcome Measures

    1. in hospital all cause morality [hospital discharge up to 90 days]

    Secondary Outcome Measures

    1. 28 day mortality [28 day]

    2. 90 day all cause mortality [90 day]

    3. 6 month all cause mortality [180 days]

    4. mechanical ventilation free days [hospital discharge up to 90 days]

    5. intensive care unit free days [hospital discharge up to 90 days]

    6. proportion of patients with secondary infections [hospital discharge up to 90 days]

    7. proportion of patients who require ECMO [hospital discharge up to 90 days]

    8. respiratory function and health status [180 days]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years and Older
    Sexes Eligible for Study:
    All
    Accepts 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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Raymond Poincaré hospital Garches France 92380

    Sponsors and Collaborators

    • University of Versailles
    • Assistance Publique - Hôpitaux de Paris

    Investigators

    • Study Chair: Djillali Annane, MD,PhD, AP--HP and University of Versailles SQY
    • Principal Investigator: Christian Brun Buisson, MD, AP-HP and Paris XII University
    • Principal Investigator: Charles Mayaud, AP-HP and University of Paris VII
    • Principal Investigator: Bernard Régnier, AP-HP and Paris VII University
    • Principal Investigator: Christian Perronne, AP-HP and University of Versailles SQY

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Djillali Annane, Dean of the health Science Centre, University of Versailles
    ClinicalTrials.gov Identifier:
    NCT01014364
    Other Study ID Numbers:
    • PCR09006
    First Posted:
    Nov 17, 2009
    Last Update Posted:
    Dec 18, 2014
    Last Verified:
    Dec 1, 2014

    Study Results

    No Results Posted as of Dec 18, 2014