A Study to Evaluate the Safety of DAYVIGO (Lemborexant) Tablets in Participants With Insomnia.

  • STATUS
    Recruiting
  • End date
    Mar 31, 2022
  • participants needed
    300
  • sponsor
    Eisai Co., Ltd.
Updated on 4 August 2021
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Eisai trial site 10 (6.1 mi away) Contact
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Summary

The purpose of the study is to evaluate the incidence of somnolence, parasomnia, narcoleptic symptoms, and suicidal ideation/suicidal behavior after administration of lemborexant (DAYVIGO) in daily practice.

Details
Condition Insomnia
Treatment Lemborexant
Clinical Study IdentifierNCT04573556
SponsorEisai Co., Ltd.
Last Modified on4 August 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Participants who are treated with lemborexant
Participants who provide consent for participation in the study
Participants who were registered in EDC by 14 days after DAYVIGO treatment initiation

Exclusion Criteria

Participants who were enrolled in this study before obtaining informed consent of this study
Participants who were participating in a clinical trial at the time of this study
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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