Genomic Tools for Studying the Ecology of the Human Vaginal Microflora
NCT ID: NCT00576797
Last Updated: 2016-02-02
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
396 participants
OBSERVATIONAL
2008-05-31
2009-01-31
Brief Summary
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Detailed Description
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Four hundred women will be recruited such that there will be equal distribution among four self-declared ethnic groups (Caucasian, African-American, Hispanic and Asian). These groupings were selected based on the original Forney study that identified different distributions supergroups of dominant vaginal microflora between African-American and Caucasian women.
The experimental focus of this proposal is to use a combination of culture-independent methods (T-RFLP of 16S rRNA, 16SrRNA and recA genes sequence analysis and community genomics) to develop tools aimed at advancing our understanding of the composition and role of individual organisms and communities that make up the ecosystems of human vaginas . The specific aims are designed to develop genomic tools for the research and clinical scientific community to study the ecology of the human vaginal microflora
Conditions
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Study Design
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PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Regular menstrual cycles from 21 to 35 days long
* Normal healthy volunteer
* Negative urine pregnancy test
* Ability to understand and sign informed consent
Exclusion Criteria
* Sexually active in the past 48 hours (involving female genitalia)
* Pregnancy (by history or testing)
* Use of antibiotics or antifungal drugs within the past 30 days
* Have chronic illnesses such as kidney failure, diabetes or HIV/AIDS
* Self-reported vaginal discharge in the past 48 hours
* Currently menstruating
* Currently participating in a drug or treatment clinical research trial
* Received a vaccine within the last 30 days
* Received a vaccine against a bacterial infection
* Currently using NuvaRing for contraception
* Any other condition that in the opinion of the investigator would place the subject in unacceptable risk for participation in the study
12 Years
45 Years
FEMALE
Yes
Sponsors
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University of Maryland
OTHER
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Emory University
OTHER
Responsible Party
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Kevin Ault, MD
Principal Investigator
Principal Investigators
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Jacques Ravel, phD
Role: PRINCIPAL_INVESTIGATOR
University of Maryland
Locations
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Emory University
Atlanta, Georgia, United States
Adolescent and Young Adult Center (AYAC),UMB
Baltimore, Maryland, United States
Center for Vaccine Development, University of Maryland
Baltimore, Maryland, United States
Countries
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Other Identifiers
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IRB00001794
Identifier Type: -
Identifier Source: org_study_id
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