A prospective study of the effects of Ninjin'yoeito on anemia and depressive symptoms in postpartum wome
Not Applicable
- Conditions
- Postpartum anemia
- Registration Number
- JPRN-UMIN000044116
- Lead Sponsor
- Fukuda Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- Female
- Target Recruitment
- 1000
Inclusion Criteria
Not provided
Exclusion Criteria
(1) Patients having past history of aldosteronism, myopathy, liver dysfunction, or jaundice. (2)Patients whom investigators consider to be ineligible.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change of hemoglobin levels, Prevalence of depressive symptoms as determined by the Edinburgh Postnatal Depression Scale(EPDS)
- Secondary Outcome Measures
Name Time Method Change of fatigue(NRS)