Real-World Observational Study on Patient-Reported Outcomes in the Treatment of Insomnia with Daridorexant in Canada

NCT06311864 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2025-03-17

No results posted yet for this study

Summary

The purpose of this observational study is to evaluate the impact of daridorexant on quality of life, work productivity and insomnia symptoms in Canadian adults suffering from insomnia.

Conditions

Interventions

DRUG

Daridorexant 50 mg

As indicated by the physician

Sponsors & Collaborators

  • Idorsia Pharmaceuticals Ltd.

    collaborator INDUSTRY
  • PeriPharm

    lead OTHER

Principal Investigators

  • Jean Lachaine, PhD · PeriPharm

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-20
Primary Completion
2025-10-31
Completion
2025-10-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06311864 on ClinicalTrials.gov