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Lemborexant Shift Work Treatment Study

Effect of a Dual Orexin Receptor Antagonist, Lemborexant, on Total Sleep Time in Shift Workers: a Randomized Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05344443
Enrollment
29
Registered
2022-04-25
Start date
2022-03-10
Completion date
2024-11-30
Last updated
2026-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shift-Work Related Sleep Disturbance

Keywords

Shift Work, Daytime Sleepiness, Lemborexant

Brief summary

Insomnia and daytime sleepiness are common complaints among night shift workers, but effective sleep treatments in shift workers are lacking. The aim of this Phase IV double-blind, placebo-controlled, randomized study is to test whether a dual orexin antagonist, Lemborexant (5mg or 10mg), which would be expected to block the clock-driven orexin-mediated wakefulness during the day, will increase daytime sleep time in shift workers who complain of difficulty sleeping during the daytime compared to placebo.

Detailed description

Insomnia and daytime sleepiness are common complaints among night shift workers. A meta-analysis on sleep in shift workers indicates that fixed night shift workers sleep, on average, 0.4 hours less than fixed day shift workers, while rotating shift workers sleep on average 1 hour less than fixed day shift workers. While there may be several reasons for sleep difficulties and sleep loss among shift workers, the misalignment of one's sleep preference (i.e., goal of sleeping during the day) and one's circadian rhythm (i.e., endogenous rhythm that signals the body to be awake during the day) is thought to be a primary cause. Insufficient sleep among night shift and rotating shift workers is linked with significant health consequences, including elevated risk for cardiovascular disease and cancer. Effective sleep treatments in shift workers are lacking. However, a recent randomized study of Suvorexant (20mg), a hypocretin/orexin receptor antagonist, produced a significant improvement in daytime total sleep time compared to placebo. Available evidence suggests that the reason Suvorexant is effective is because it blocks the hypocretin/orexin receptors that mediate signaling from the biological clock (suprachiasmatic nucleus of the hypothalamus) attempting to maintain sustained wakefulness during the biological day. As Lemborexant is also a hypocretin/orexin antagonist, it would also be expected to improve daytime sleep in shift workers but would have the advantage over Suvorexant of being highly effective in the dosages available for clinical use. As such, Lemborexant is ideally positioned to be an effective and important treatment of sleep problems in shift workers. The aim of this Phase IV double-blind, placebo-controlled, randomized study is to test whether a dual orexin antagonist, Lemborexant (5mg or 10mg), which would be expected to block the clock-driven orexin-mediated wakefulness during the day, will increase daytime sleep time in shift workers who complain of difficulty sleeping during the daytime compared to placebo. This will be a 4-week double blinded placebo controlled trial (2 weeks of baseline assessment followed by 2-weeks of treatment/placebo). The trial design is based on a recent successful study of the treatment of sleep problems in shift workers with a hypocretin/orexin receptor antagonist.

Interventions

DRUGLemborexant

A dual orexin antagonist

DRUGPlacebo

A placebo that looks and tastes like Lemborexant tablets

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

This will be a 4-week double blinded placebo controlled trial (2 weeks of baseline assessment followed by 2-weeks of treatment/placebo). The trial design is based on a recent successful study of the treatment of sleep problems in shift workers with a hypocretin/orexin receptor antagonist

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Full-time night shift work (at least 6 hours per shift, 4 days per week or 32 hours per week) * Employed as a night shift worker for at least 3 months * Self-reported concerns about daytime sleepiness and difficulty sleeping during the daytime

Exclusion criteria

* Pregnancy (verified by urine pregnancy test) or plan to become pregnant in the next 3 months * Currently breastfeeding * Inadequate opportunity for sleep during the daytime (\< 7 hours opportunity) after overnight shift * Extreme circadian preference (based on Horne \& Ostberg Morningness-Eveningness Questionnaire) * Severe depressive symptoms (\>25 on CES-D) * Unwillingness to discontinue sleep aids (prescription or non-prescription) during the study period * Presence of sleep disordered breathing (verified by Apnea link) * Self-reported diagnosis of narcolepsy, restless legs syndrome * Self-reported intake of \>600mg of caffeine per night shift or use of stimulants during night shift, rotational, or irregular shifts * Unstable or untreated medical or psychiatric condition based on clinical interview. * Severe hepatic or renal impairment (based on chemistry panel); * Self-reported use of digoxin or strong or moderate cytochrome P450 3A4 isozyme inhibitors or cytochrome P450 3A4 isozyme inducers for 6 months prior to or during the study

Design outcomes

Primary

MeasureTime frameDescription
Daytime Total Sleep Time in Minutes Per Day Collected From the Consensus Sleep DiaryTwo weeks of TreatmentDaytime total sleep time in minutes per day following a night shift averaged over the two-week treatment/placebo period. Daytime total sleep time in minutes per day was recorded using the Consensus Sleep Diary, which participants completed daily.

Secondary

MeasureTime frameDescription
Daytime Total Sleep Time in Minutes Per Day Measured by ActigraphyTwo weeks of treatmentDaytime total sleep time in minutes per day following a night shift averaged over the two-week treatment/placebo period. Daytime total sleep time in minutes per day was collected using daily actigraphy data from Actiwatches, which participants wore during the two week treatment period.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORAric Prather, PhD

University of California, San Francisco

Participant flow

Recruitment details

Recruitment of participants began in March 2022 and ended in December 2024. Participants were recruited primarily through flyers, with targeted recruitment at local hospitals.

Pre-assignment details

Study participants completed baseline assessments, including sociodemographic questionnaires, clinical labs, and sleep measures (diaries, actigraphy) prior to randomization.

Baseline characteristics

Characteristic
Actigraphy-based daytime total sleep time286.4 Minutes per day
STANDARD_DEVIATION 59.8
Age, Continuous37.2 Years
STANDARD_DEVIATION 8.7
Diary-based daytime total sleep time341.1 Minutes per day
STANDARD_DEVIATION 78.9
Race/Ethnicity, Customized
Asian
7 Participants
Race/Ethnicity, Customized
Black/African American
3 Participants
Race/Ethnicity, Customized
Hispanic/Latino
4 Participants
Race/Ethnicity, Customized
Multiracial
0 Participants
Race/Ethnicity, Customized
White/Caucasian
8 Participants
Region of Enrollment
United States
14 Participants
Sex: Female, Male
Female
13 Participants
Sex: Female, Male
Male
1 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 150 / 14
other
Total, other adverse events
5 / 151 / 14
serious
Total, serious adverse events
0 / 150 / 14

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026