Cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients with cancer(more than or equal to 80%) 2.Patients with delirium 3.Trials including combined antipsychotic and antihistamine therapy 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 |
|---|---|
| Change in severity of delirium before and after treatment initiation | — |
Secondary
| Measure | Time frame |
|---|---|
| somnolence, extrapyramidal signs and QT prolongation | — |
Countries
Japan
Contacts
IMSUT Hospital, the Institute of Medical Science, The University of Tokyo Department of Palliative Medicine and Advanced Clinical Oncology