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
189 participants
OBSERVATIONAL
2008-02-29
2012-01-31
Brief Summary
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Detailed Description
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Women with PCOS may be eligible to participate in this study if they are between the ages of 18 and 50 and have two living biological parents who are also willing to participate. Study participation involves telephone screening and consent and home collection by subjects (probands) and their parents of sputum (saliva) in a provided container. Specimen containers and signed consent forms will be returned to the study site by mail.
The major goal of this research project, the identification of genes contributing to PCOS, will provide basic understanding of the genotype-phenotype relationships that contribute to features of PCOS. Knowledge of "PCOS genes" would assist physicians in predicting and assessing responses to interventions that promote fertility, improve insulin sensitivity, and treat other aspects of the disease.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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1
Women with diagnosis of PCOS
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Both biological parents alive
* Yes to both answers and parents willing to participate
Exclusion Criteria
FEMALE
No
Sponsors
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University of Iowa
OTHER
University of Pennsylvania
OTHER
Responsible Party
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Principal Investigators
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Anuja Dokras-Jagasia, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Pennsylvania
Brad V Voorhis, MD
Role: PRINCIPAL_INVESTIGATOR
University of Iowa
Locations
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University of Pennsylvania
Philadelphia, Pennsylvania, United States
Countries
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Other Identifiers
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University of IOWA# 200707772
Identifier Type: -
Identifier Source: secondary_id
807101
Identifier Type: -
Identifier Source: org_study_id
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