Clinical trial design in prevention and treatment of acute respiratory distress syndrome.

Abstract:

:Our ability to define appropriate molecular targets for preclinical development and develop better methods needs to be improved, to determine the clinical value of novel acute respiratory distress syndrome (ARDS) agents. Clinical trials must have realistic sample sizes and meaningful end points and use the available observation and meta-analytical data to inform design. Biomarker-driven studies or defined ARDS subsets should be considered to categorize specific at-risk populations most likely to benefit from a new treatment. Innovations in clinical trial design should be pursued to improve the outlook for future interventional trials in ARDS.

journal_name

Clin Chest Med

authors

Curley GF,McAuley DF

doi

10.1016/j.ccm.2014.08.009

subject

Has Abstract

pub_date

2014-12-01 00:00:00

pages

713-27

issue

4

eissn

0272-5231

issn

1557-8216

pii

S0272-5231(14)00078-1

journal_volume

35

pub_type

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