Efficacy of ramelteon on sleep disturbance and restlessness in acute stroke
Not Applicable
- Conditions
- stroke
- Registration Number
- JPRN-UMIN000012755
- Lead Sponsor
- Yokohama Sakae Kyosai Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients taking ramelteon at the time of admission 2.Patients with contraindication for ramelteon (known hypersensitivity to remelteon, a history of severe liver/hepatic dysfunction, patients taking fluvoxamine maleate) 3.Patients who were not able to take drug both orally and through the tube
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Richmond agitation sedation scale two weeks after intervention
- Secondary Outcome Measures
Name Time Method sleep condition/ insomnia/ daytime somnolence/ administration of sedative medication, psychotropic medication and sleep medication except for ramelteon/ body restraint/ fall/ modified Rankin Scale/ adverse events