delirium
Conditions
Interventions
suvolexant
placebo
Sponsors
Juntendo University
Nippon Medical School Musashikosugi Hospital Hiroshima City Hospital Tokyo Medical and Dental University Kanazawa University Graduate School of Medical Science
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients newly admitted due to emergency, and able to take medicine orally
Exclusion criteria
Exclusion criteria: Patients who have an expected stay or life expectancy less than 2 night
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of delirium as determined by the DSM-5. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Estimates of the probability of developing delirium 2. Change in inflammatory markers | — |
Countries
Japan
Contacts
Public ContactKotaro Hatta
Juntendo University Nerima Hospital Department of Psychiatry
Outcome results
None listed