Apply to trial NCT06874855

A few quick questions so the study team can decide if you might be a fit.

RecruitingPhase 4Drug trial

Lemborexant in Delayed Sleep Phase Syndrome

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.

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  3. The team reaches out to schedule screening

    Usually within a few business days, via the contact you give.

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