02656nas a2200373 4500000000100000008004100001653001100042653002000053653001000073653002500083653002300108100001500131700001700146700002000163700001900183700001800202700002000220700001900240700002000259700001500279700002000294700001400314700001900328700002000347700001600367700001700383700001600400700003700416245016200453300001000615490000700625520163600632022001402268 2017 d10aHumans10aResearch Design10aFever10aIntensive Care Units10aClinical Protocols1 aYoung Paul1 aSaxena Manoj1 aBellomo Rinaldo1 aFreebairn Ross1 aHammond Naomi1 aHenderson Seton1 aMcArthur Colin1 aMcGuinness Shay1 aWebb Steve1 aBeasley Richard1 aMyburgh J1 aBailey Michael1 avan Haren Frank1 aHarward Meg1 aMackle Diane1 aTurner Anne1 aThe ANZICS Clinical Trials Group00aProtocol and statistical analysis plan for the Randomised Evaluation of Active Control of Temperature versus Ordinary Temperature Management (REACTOR) trial. a81-870 v193 a

BACKGROUND: Body temperature can be reduced in febrile patients in the intensive care unit using medicines and physical cooling devices, but it is not known whether systematically preventing and treating fever reduces body temperature compared with standard care.

OBJECTIVE: To describe the study protocol and statistical analysis plan for the Randomised Evaluation of Active Control of Temperature versus Ordinary Temperature Management (REACTOR) trial.

DESIGN, SETTING AND PARTICIPANTS: Protocol for a phase II, multicentre trial to be conducted in Australian and New Zealand ICUs admitting adult patients. We will recruit 184 adults without acute brain injury who are expected to be ventilated in the ICU beyond the day after randomisation. We will use open, random, parallel assignment to systematic prevention and treatment of fever, or to standard temperature management.

MAIN OUTCOME MEASURES: The primary end point will be mean body temperature, calculated from body temperatures measured 6-hourly for 7 days (168 hours) or until ICU discharge, whichever is sooner. Secondary end points are ICU-free days, in-hospital and cause-specific mortality (censored at Day 90) and survival time to Day 90 (censored at hospital discharge).

RESULTS AND CONCLUSIONS: The trial will determine whether active temperature control reduces body temperature compared with standard care. It is primarily being conducted to establish whether a phase III trial with a patient-centred end point of Day 90 mortality is justified and feasible.

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