A multicenter prospective observational study on the structured psychotropic drugs intervention for hyperactive delirium in terminally-ill cancer patients
Not Applicable
- Conditions
- Cancer
- Registration Number
- JPRN-UMIN000040146
- Lead Sponsor
- Seirei Mikatahara General Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patients for whom psychotropic drugs are contraindicated. 2) Patients who indicated that they would refuse to participate in this study. 3) Patients judged to be inappropriate by the attending physician.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The proportion of patients receiving structured psychotropic drugs intervention for hyperactive/mixed delirium at 3 days after (T2). If not, the reason for discontinuation.
- Secondary Outcome Measures
Name Time Method