Insomnia
Conditions
Interventions
Receiving suvorexant 20 mg
Receiving lormetazepam 2 mg
Receiving placebo
Sponsors
Fukushima Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Healthy participants aged 20 years and older
Exclusion criteria
Exclusion criteria: History of mental illness and neurological disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Individual mean amplitudes of mismatch negativity (MMN) and P300 1 day after oral administration of lormetazapam and suvorexant. | — |
Countries
Japan
Contacts
Public ContactTetsuya Shiga
Fukushima Medical University Department of Neuropsychiatry
Outcome results
None listed