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Characteristics of Women With Reproductive Concerns

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ClinicalTrials.gov Identifier: NCT02429336
Recruitment Status : Recruiting
First Posted : April 29, 2015
Last Update Posted : October 26, 2017
Sponsor:
Information provided by (Responsible Party):
University of Tennessee

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
Endocrine Disorders of Female Reproductive System

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 Type : Observational
Estimated Enrollment : 200 participants
Observational Model: Case-Control
Time Perspective: Prospective
Official Title: Clinical Characteristics of Women Presenting to the Reproductive Endocrinology Clinic
Study Start Date : January 2012
Estimated Primary Completion Date : August 2020
Estimated Study Completion Date : August 2022



Primary Outcome Measures :
  1. Data collection from patients' charts. [ Time Frame: up to 1 year from the time of signing the informed consent for data collection ]
    Data collection from patients' charts.



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Ages Eligible for Study:   8 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Population: All patients presenting to the reproductive endocrinology clinic.
Criteria

Inclusion Criteria:

  • females of childbearing potential experiencing reproductive endocrinology related problems

Exclusion Criteria:

  • male or female not of childbearing potential

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02429336


Contacts
Contact: Laura Detti, M.D. 901-448-1622 ldetti@uthsc.edu
Contact: Annette B. Hickerson, RN 901-448-4784 abpayne@uthsc.edu

Locations
United States, Tennessee
Regional One Health Ob-Gyn Clinic Recruiting
Memphis, Tennessee, United States, 38103
Contact: Annette B. Hickerson, R.N.    901-448-4784    abpayne@uthsc.edu   
Sub-Investigator: Ana Tobiasz, M.D.         
Sub-Investigator: Shelby Osborne, M.D.         
Sponsors and Collaborators
University of Tennessee
Investigators
Principal Investigator: Laura Detti, M.D. Associate Professor, UTennessee Health Science Center

Responsible Party: University of Tennessee
ClinicalTrials.gov Identifier: NCT02429336     History of Changes
Other Study ID Numbers: 11-01368-XP
First Posted: April 29, 2015    Key Record Dates
Last Update Posted: October 26, 2017
Last Verified: October 2016

Additional relevant MeSH terms:
Endocrine System Diseases