Safety and efficacy of scallop-plasmalogen on patients with primary insomnia:double-blind crossover trial with Polysomnography
Not Applicable
- Conditions
- primary insomnia
- Registration Number
- JPRN-UMIN000021337
- Lead Sponsor
- BOOCS Clinic Fukuoka
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 16
Inclusion Criteria
Not provided
Exclusion Criteria
1.Patients with depression, history of severe mental or physical illness, or sleep disorder other than insomnia (sleep apnea syndrome, restless legs syndrome) 2.Patients with scallop allergy 3.Patients judged ineligible for this study by the investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement of wake after sleep onset
- Secondary Outcome Measures
Name Time Method Improvement of sleep efficiency and sleep latency