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Characteristics of Women With Reproductive Concerns

Sponsor
University of Tennessee (Other)
Overall Status
Completed
CT.gov ID
NCT02429336
Collaborator
(none)
194
Enrollment
1
Location
101.9
Duration (Months)
1.9
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to collect data that will be generated during an office visit. The data will be gathered and analyzed in research studies that will help with the investigators understanding of various medical conditions.

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.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Purpose: To collect the characteristics of patients presenting to the reproductive endocrinology clinic.

    Rationale: Patients' characteristics will be analyzed as part of clinical research studies and may help in understanding the causes of their condition.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    194 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Clinical Characteristics of Women Presenting to the Reproductive Endocrinology Clinic
    Study Start Date :
    Jan 1, 2012
    Actual Primary Completion Date :
    Jun 30, 2020
    Actual Study Completion Date :
    Jun 30, 2020

    Outcome Measures

    Primary Outcome Measures

    1. Data collection from patients' charts. [up to 1 year from the time of signing the informed consent for data collection]

      Data collection from patients' charts.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    8 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • females of childbearing potential experiencing reproductive endocrinology related problems
    Exclusion Criteria:
    • male or female not of childbearing potential

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Regional One Health Ob-Gyn Clinic Memphis Tennessee United States 38103

    Sponsors and Collaborators

    • University of Tennessee

    Investigators

    • Principal Investigator: Laura Detti, M.D., Associate Professor, UTennessee Health Science Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Tennessee
    ClinicalTrials.gov Identifier:
    NCT02429336
    Other Study ID Numbers:
    • 11-01368-XP
    First Posted:
    Apr 29, 2015
    Last Update Posted:
    Nov 13, 2020
    Last Verified:
    Nov 1, 2020
    Additional relevant MeSH terms:
    Endocrine System Diseases

    Study Results

    No Results Posted as of Nov 13, 2020