Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
4000 participants
OBSERVATIONAL
2009-02-28
2012-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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1
Psychoses within the first 3 months postpartum
No interventions assigned to this group
2
Psychoses \> 3 months to 6 months postpartum
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Chinese
Exclusion Criteria
* Gestational age \< 32 weeks
18 Years
50 Years
FEMALE
No
Sponsors
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Nanjing Medical University
OTHER
Responsible Party
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Fu Zhou Wang
Dr
Principal Investigators
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XiaoFeng Shen, MD
Role: STUDY_DIRECTOR
Nanjing Medical University
Locations
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Nanjing Maternal and Child Health Care Hospital
Nanjing, Jiangsu, China
Countries
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Other Identifiers
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NJFY09102M107
Identifier Type: -
Identifier Source: secondary_id
NMU-200903-MZ003
Identifier Type: -
Identifier Source: org_study_id
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