The Study of Polycystic Ovary Syndrome (PCOS) and Questionnaire
NCT ID: NCT01256970
Last Updated: 2013-09-11
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
306 participants
OBSERVATIONAL
2010-11-30
2013-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Polycystic Ovary Syndrome.
Polycystic ovary syndrome was diagnosed according to the 2003 Rotterdam criteria, which require a minimum of two of the following three criteria: PCOM, chronic anovulation and hyperandrogenism.
No interventions assigned to this group
Normal Control
Normal control women were women who did not present with any of three PCOS criteria.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* women with PCOS and women without PCOS
Exclusion Criteria
* women older than 45 years old, Amenorrhea of menopause, hyperglycemia, hyperthyroidism, hypothyroidism, heart failure, lung failure, renal failure, anemia, dystrophy, gonitis
15 Years
45 Years
FEMALE
Yes
Sponsors
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Taipei Medical University WanFang Hospital
OTHER
Responsible Party
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Ming-I Hsu
Attending Doctor
Principal Investigators
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Ming-I Hsu
Role: PRINCIPAL_INVESTIGATOR
Taipei Medical University WanFang Hospital
Locations
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Taipei Medical University-WanFang Hospital
Taipei, , Taiwan
Countries
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Other Identifiers
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WFH-PCOS-99075
Identifier Type: -
Identifier Source: org_study_id