drugset / Trial / NCT06231641

The Effects of Lemborexant on the Ability to Sleep During Daytime

NCT06231641 ↗

RandomizedCrossoverDouble-blindTreatment

Summary

This study aim to evaluate whether a dose of 5 mg of lemborexant, as compared to a placebo, may improve daytime recovery sleep, without producing lingering sleepiness during wakefulness, using a 3-day simulated night shift protocol in the lab under constant monitoring.

Timeline

Start
2024-01-11
Primary completion
2026-03-31
Completion
2026-03-31

Outcome

Outcome not reported

Stopped (Enrollment): “In agreement with all parties, the project was closed on March 31 due to recruitment challenges.”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lemborexant Small molecule 5 mg Oral