Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2004 Jul;174(3):421-9.
doi: 10.1007/s00213-003-1759-5. Epub 2004 Mar 17.

Sleep-promoting properties of quetiapine in healthy subjects

Affiliations
Clinical Trial

Sleep-promoting properties of quetiapine in healthy subjects

Stefan Cohrs et al. Psychopharmacology (Berl). 2004 Jul.

Abstract

The aim of this study was to investigate the effects of quetiapine, an atypical antipsychotic, on polysomnographic sleep structure and subjective sleep quality. This double-blind, placebo-controlled, randomized cross-over study investigated the polysomnographic sleep structure and subjective sleep quality of 14 healthy male subjects given placebo, quetiapine 25 mg or quetiapine 100 mg. Volunteers were studied 3 times for 3 consecutive nights (N0, adaptation; N1, standard sleep conditions; N2, acoustic stress) 4 days apart. Treatment was administered orally 1 h before bedtime on nights 1 and 2. Quetiapine 25 mg and 100 mg significantly improved sleep induction and continuity under standard and acoustic stress conditions. Increases in total sleep time, sleep efficiency, percentage sleep stage 2 and subjective sleep quality were seen. A significant increase in periodic leg movements during sleep was observed with quetiapine 100 mg. The sleep-improving properties of quetiapine may be important in counteracting different aspects of psychopathology in schizophrenia and other disorders. These sleep-inducing and sleep-modifying properties are probably related to quetiapine's receptor-binding profile, including its antihistaminergic, antidopaminergic and antiadrenergic properties. Other mechanisms might be relevant as well and further investigation is required.

PubMed Disclaimer

References

    1. Biol Psychiatry. 1991 Nov 1;30(9):904-12 - PubMed
    1. J Clin Psychopharmacol. 1995 Apr;15(2):132-7 - PubMed
    1. Biol Psychiatry. 1997 Aug 15;42(4):260-6 - PubMed
    1. Biol Psychiatry. 1999 Jul 1;46(1):141-3 - PubMed
    1. Pharmacopsychiatry. 2001 Jul;34(4):150-4 - PubMed

Publication types

LinkOut - more resources