Design, conduct, analysis and reporting of a multi-national placebo-controlled trial of activated protein C for persistent septic shock

Intensive Care Medicine - Tập 34 - Trang 1935-1947 - 2008
Simon Finfer1, V. Marco Ranieri2, B. Taylor Thompson3, Philip S. Barie4, Jean-François Dhainaut5, Ivor S. Douglas6, Bengt Gårdlund7, John C. Marshall8, Andrew Rhodes9
1Critical Care and Trauma, The George Institute for International Health, University of Sydney, Sydney, Australia
2Ospedale S. Giovanni Battista-Molinette, Università di Torino, Torino, Italy
3Pulmonary and Critical Care Unit, Bullfinch Building, Room 148, Massachusetts General Hospital, Boston, USA
4Department of Surgery, P713A Weill Cornell Medical College, New York, USA
5Cochin Port Royal Hospital-Paris Descartes University, Paris, France
6Denver Health and University of Colorado, Denver, USA
7Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden
8Departments of Surgery and Critical Care Medicine, St Michael’s Hospital, Toronto, Canada
9Department of Intensive Care Medicine and Anaesthesia, St George’s Hospital, London, UK

Tóm tắt

The role of drotrecogin alfa (activated) (DAA) in severe sepsis remains controversial and clinicians are unsure whether or not to treat their patients with DAA. In response to a request from the European Medicines Agency, Eli Lilly will sponsor a new placebo-controlled trial and history suggests the results will be subject to great scrutiny. An academic steering committee will oversee the conduct of the study and will write the study manuscripts. The steering committee intends that the study will be conducted with the maximum possible transparency; this includes publication of the study protocol and a memorandum of understanding which delineates the role of the sponsor. The trial has the potential to provide clinicians with valuable data but patients will only benefit if clinicians have confidence in the conduct, analysis and reporting of the trial. This special article describes the process by which the trial was developed, major decisions regarding trial design, and plans for independent analysis, interpretation and reporting of the data.

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