Lemborexant in Delayed Sleep Phase Syndrome

Recruiting Phase 4 Interventional Study
Delayed Sleep Phase Syndrome
Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
15 (estimated)
Sponsor
University of California, San Francisco · Other
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About This Trial
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 p…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: \- Participants will be required to be 18 years of age or older and have delayed sleep phase syndrome (DSPS). Questionnaires will be used to identify potential confounders and to confirm a potential diagnosis of DSPS based on ICSD3 criteria: a) Sleep is delayed by two hours or m…
Contacts

Andrew D Krystal, MD, MS

415-476-7702

andrew.krystal@ucsf.edu

CONTACT