Cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients with cancer (more than or equal to 80%) 2.Patients without delirium before intervention 3.Studies examining the efficacy or safety of Ramelteon for the prevention of delirium in adult cancer patients The study design to be considered for inclusion is as follows: 1.If there were at least two randomized controlled trial (RCT)s, inclusion was completed. 2.If there were less than 2 RCTs, we included non-RCTs or observational studies with control groups. 3.If there were no RCTs/non-RCTs/observational studies with control groups, single-arm observational studies were considered for inclusion.
Exclusion criteria
Exclusion criteria: 1.Duplicate publications 2.Conference proceedings
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Delirium incidence | — |
Secondary
| Measure | Time frame |
|---|---|
| delirium severity, somnolence, tumbling and falls | — |
Countries
Japan
Contacts
National Cancer Center Division of Quality Assurance Programs