Skip to content

Intravenous chlorpromazine for the treatment of insomnia in end-stage cancer patients with difficulty in oral administration

Intravenous chlorpromazine for the treatment of insomnia in end-stage cancer patients with difficulty in oral administration - Intravenous chlorpromazine for the treatment of insomnia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000029365
Enrollment
30
Registered
2017-10-01
Start date
2015-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

sleep disturbance

Interventions

None listed

Sponsors

Kansai Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime 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

Public ContactHideaki Hasuo

Kansai Medical University Department of Psychosomatic Medicine

hasuohid@hirakata.kmu.ac.jp072-804-0101

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026