Evaluating Factors That Impact Loss to Follow-up Among Postpartum HIV-infected Women in Mississippi
NCT ID: NCT01190605
Last Updated: 2014-12-09
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
53 participants
OBSERVATIONAL
2010-07-31
2013-07-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
* women with HIV infection who are pregnant or up to 2 months postpartum
* English speaking
* able to give informed consent
18 Years
45 Years
FEMALE
No
Sponsors
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Brown University
OTHER
University of Mississippi Medical Center
OTHER
Responsible Party
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Binford Nash
Asst. Professor, Pediatrics, School of Medicine
Principal Investigators
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Binford T Nash, MD
Role: PRINCIPAL_INVESTIGATOR
University of Mississippi Medical Center
Locations
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University of Mississippi Medical Center
Jackson, Mississippi, United States
Countries
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Other Identifiers
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2010-0131
Identifier Type: -
Identifier Source: org_study_id