sleep disturbance
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Study subjects were 30 end-stage cancer patients with difficulty in oral administration from whom the informed consent for intravenous chlorpromazine was obtained.
Exclusion criteria
Exclusion criteria: We focused on only primary insomnia excluding secondary insomnia attributed to delirium or medications. The study excluded psychiatric disorder patients with difficulty in communication such as dementia.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary endpoint in this study was sleep quality based on St. Marys Hospital Sleep Questionnaire 3 days after the chlorpromazine treatment as a chlorpromazine efficacy index. | — |
Countries
Japan
Contacts
Kansai Medical University Department of Psychosomatic Medicine