Japan PHarmacological Audit study of Safety and Efficacy in Realworld (Phase-R) Delirium Study
Not Applicable
- Conditions
- Malignancy
- Registration Number
- JPRN-UMIN000018589
- Lead Sponsor
- The University of Tokyo, The Institute of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 1000
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with substance withdrawal delirium Patient with postoperative delirium Patients who undergo medical treatments intended to terminal sedation
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method