Condition: Delayed Sleep Phase Syndrome · Sponsor: University of California, San Francisco
The purpose of the study is to evaluate whether Lemborexant is more effective than placebo in shortening sleep onset latency in patients with delayed sleep phase syndrome (both type 1 and type 2). This will be tracked using sleep logs as well as actigraphy. In this 2-year study, the investigators will examine if Lemborexant administered 5-10 mg nightly taken at desired bedtime (at least 2 hours prior to self-reported sleep onset habitual time) can improve the symptoms of Delayed Sleep Phase Syndrome.
This description comes directly from the study's public registry record.
Andrew D Krystal, MD, MS · 415-476-7702 · andrew.krystal@ucsf.edu
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| University of California San Francisco | San Francisco, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06874855