A pilot study for the efficacy of the non-benzodiazepine hypnotic or orexin receptor antagonist on insomnia in major depressive patients unresponsive to benzodiazepine hypnotic treatment: a randomized open-label trial.
Not Applicable
- Conditions
- major depressive disorder
- Registration Number
- JPRN-UMIN000031032
- Lead Sponsor
- Department of Clinical Pharmacology and Therapeutics, Kyoto University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1. Patients taking other hypnotics. 2. Patients judged not to be accurately taken. 3. Patients with severe physical disease. 4. Patients with a history of severe drug hypersensitivity or drug allergy. 5. Women who are pregnant or who wish to be pregnant during the study period, and lactating mother. 6. Patients taking agents causing insomnia. 7. Patients judged to be high-risk for substance abuse. 8. Patients judged to be high risk for suicide. 9. Patients judged to be inappropriate for participation by researchers.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method