@article{22971, keywords = {Humans, Research Design, Fever, Intensive Care Units, Clinical Protocols}, author = {Young Paul and Saxena Manoj and Bellomo Rinaldo and Freebairn Ross and Hammond Naomi and Henderson Seton and McArthur Colin and McGuinness Shay and Webb Steve and Beasley Richard and Myburgh J and Bailey Michael and van Haren Frank and Harward Meg and Mackle Diane and Turner Anne and The ANZICS Clinical Trials Group}, title = {Protocol and statistical analysis plan for the Randomised Evaluation of Active Control of Temperature versus Ordinary Temperature Management (REACTOR) trial.}, abstract = {
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.
}, year = {2017}, journal = {Crit Care Resusc}, volume = {19}, pages = {81-87}, issn = {1441-2772}, language = {eng}, }