Publication: Study protocol for a randomised controlled trial evaluating the effects of the orexin receptor antagonist suvorexant on sleep architecture and delirium in the intensive care unit
Issued Date
2020-07-19
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20446055
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2-s2.0-85088426797
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Mahidol University
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SCOPUS
Bibliographic Citation
BMJ Open. Vol.10, No.7 (2020)
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Omid Azimaraghi, Maximilian Hammer, Peter Santer, Katharina Platzbecker, Friederike C. Althoff, Maria Patrocinio, Stephanie D. Grabitz, Karuna Wongtangman, Sandra Rumyantsev, Xinling Xu, Maximilian S. Schaefer, Patrick M. Fuller, Balachundhar Subramaniam, Matthias Eikermann Study protocol for a randomised controlled trial evaluating the effects of the orexin receptor antagonist suvorexant on sleep architecture and delirium in the intensive care unit. BMJ Open. Vol.10, No.7 (2020). doi:10.1136/bmjopen-2020-038474 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/58061
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Title
Study protocol for a randomised controlled trial evaluating the effects of the orexin receptor antagonist suvorexant on sleep architecture and delirium in the intensive care unit
Abstract
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. Introduction Insomnia frequently occurs in patients admitted to an intensive care unit (ICU). Sleep-promoting agents may reduce rapid eye movement sleep and have deliriogenic effects. Suvorexant (Belsomra) is an orexin receptor antagonist with Food and Drug Administration (FDA) approval for the treatment of adult insomnia, which improves sleep onset and maintenance as well as subjective measures of quality of sleep. This trial will evaluate the efficacy of postoperative oral suvorexant treatment on night-time wakefulness after persistent sleep onset as well as the incidence and duration of delirium among adult cardiac surgical patients. Methods and analysis In this single-centre, randomised, double-blind, placebo-controlled trial, we will enrol 120 patients, aged 60 years or older, undergoing elective cardiac surgery with planned postoperative admission to the ICU. Participants will be randomised to receive oral suvorexant (20 mg) or placebo one time a day starting the night after extubation. The primary outcome will be wakefulness after persistent sleep onset. The secondary outcome will be total sleep time. Exploratory outcomes will include time to sleep onset, incidence of postoperative in-hospital delirium, number of delirium-free days and subjective sleep quality. Ethics and dissemination Ethics approval was obtained through the € Committee on Clinical Investigations' at Beth Israel Deaconess Medical Center (protocol number 2019P000759). The findings will be published in peer-reviewed journals. Trial registration number This trial has been registered at clinicaltrials.gov on 17 September 2019 (NCT04092894).