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
194 participants
OBSERVATIONAL
2012-01-31
2020-06-30
Brief Summary
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About 200 subjects will be participating in this study. Participation in this study will not require a patient's time or presence. The medical information contained in a patient's chart from the office visit, including the results of any tests that were ordered at that time, will be transferred to an anonymous database and analyzed together with data from other patients who have similar condition/s.
No follow-up information will be collected. The following information will be collected from a patient's medical record: the medical history and a list of the current medications.
Detailed Description
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Rationale: Patients' characteristics will be analyzed as part of clinical research studies and may help in understanding the causes of their condition.
Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
8 Years
FEMALE
No
Sponsors
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University of Tennessee
OTHER
Responsible Party
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Principal Investigators
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Laura Detti, M.D.
Role: PRINCIPAL_INVESTIGATOR
Associate Professor, UTennessee Health Science Center
Locations
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Regional One Health Ob-Gyn Clinic
Memphis, Tennessee, United States
Countries
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Other Identifiers
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11-01368-XP
Identifier Type: -
Identifier Source: org_study_id