Real-World Observational Study on Patient-Reported Outcomes in the Treatment of Insomnia With Daridorexant in Canada
- Sponsor
- PeriPharm
- Study ID
- NCT06311864
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Daridorexant 50 mg — DRUGAs indicated by the physician
Study Details
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.
Key Dates
- First listed
- Mar 15, 2024
- Start date
- Jun 20, 2024
- Status verified
- May 2026
- Primary completion
- May 19, 2026
- Completion
- May 19, 2026
Study Design
- Enrollment
- 90 participants (actual)
Arms
- Arm: daridorexantPatients who have been newly prescribed oral tablets of daridorexant 50 mg to treat their insomnia
Primary Outcome Measure
Change from Baseline in Quality of Life [ Time Frame: Month 1, Month 2, Month 3 ]
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