Observational study of the associations between Premenstrual Syndrome (PMS) and blood compositions
- Conditions
- Premenstrual Syndrome
- Registration Number
- JPRN-UMIN000049552
- Lead Sponsor
- IMEQRD Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- Female
- Target Recruitment
- 62
Not provided
1)Subjects who are currently pregnant or breastfeeding, and subjects who wish to become pregnant during the study period 2)Subjects taking hormonal contraceptives (including low-dose pills) 3)smoker 4)Subjects with a history of and presenting psychiatric illness 5)Subjects with surgical injuries or medical conditions that may affect study conduct 6)Subjects with iron deficiency anemia (hemoglobin <11.5g / dl) 7)Subjects who plan to change their lifestyle (eating, sleeping, exercise habits, etc.) significantly during the test period, such as long-term travel 8)Subjects who have collected more than 200 ml of blood within 12 weeks before the start of the study 9)Subjects who are judged to be inappropriate by the principal investigator
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method