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Use of Lemborexant for Insomnia in Our Clinic: A Retrospective Study

Use of Lemborexant for Insomnia in Our Clinic: A Retrospective Study - Use of Lemborexant for Insomnia in Our Clinic: A Retrospective Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000054075
Enrollment
1000
Registered
2024-04-06
Start date
2024-04-05
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Insomnia

Interventions

None listed

Sponsors

General Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who visited our clinic between April 2022 and March 2024 2.Patients diagnosed with insomnia and prescribed Lemborexant at their initial visit 3.Patients with no history of Lemborexant use prior to their first consultation 4.Adult patients aged 18 years and older

Exclusion criteria

Exclusion criteria: 1.Patients diagnosed with sleep disorders other than insomnia 2.Patients who were administered other insomnia medications or had their Lemborexant dosage changed within 4 weeks from the initial consultation

Design outcomes

Primary

MeasureTime frame
This study evaluates the impact of Lemborexant treatment on patients' sleep latency, number of nocturnal awakenings, frequency of early morning awakenings, and sleep quality. Additionally, the efficacy of Lemborexant will be assessed using the Athens Insomnia Scale (AIS).

Countries

Japan

Contacts

Public ContactHinako Imamura

General Clinic General Clinic

info@nemuri.jp0666842558

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026