Delirium prevention trial for the patients admitted in acute care ward
Not Applicable
- Conditions
- delirium
- Registration Number
- JPRN-UMIN000030104
- Lead Sponsor
- Yokohama Brain and Spine Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
Delirious patients on admission Patients with contraindication of ramelteon or suvorexant Patients who took ramelteon or suvorexant on admission
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method