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NCT06225947: PROEM

Patient-Reported Outcomes for Lemborexant in Chinese Participants With Insomnia

Status unknown Last updated 30 July 2024
What this trial tests

trial testing Lemborexant 5 MG in Insomnia in 200 participants. Status unknown.

Timeline
22 February 2024
Primary endpoint
30 March 2025
30 June 2025

Quick facts

Lead sponsorGuangdong Provincial People's Hospital
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment200
Start date22 February 2024
Primary completion30 March 2025
Estimated completion30 June 2025
Sites5 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Guangdong Provincial People's Hospital

Who can join

18 and older, any sex, with Insomnia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a prospective, open-label, single arm, multicenter study lasting 12 weeks to evaluate effectiveness and safety of lemborexant(LEM). Patient self-evaluation reports and safety events will be collected at baseline and 4 visits during treatment.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Patient-Reported Outcomes for LEMborexant Treatment in Chinese Patients with Insomnia (PROEM): A Multicenter, Prospective, Real-World Observational Study.
    Zheng S, Li X, Jian W, Tang Y, et al · · 2026 · PMID 42226892 · DOI 10.2147/nss.s596731

Verify or expand the search:

Other trials of Lemborexant 5 MG

Trials testing the same drug.

Other recruiting trials for Insomnia

Currently open trials in the same condition.

Other Guangdong Provincial People's Hospital trials

Trials by the same sponsor.

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Data sources for this page

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