Characteristics of Women With Reproductive Concerns

Completed

• Conditions: Endocrine Disorders of Female Reproductive System

• Registration Number: NCT02429336
• Lead Sponsor: 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.

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 Timeline

• Study Start: 2012-01
• Study First Submitted: 2015-03-23
• Study First Submitted QC: 2015-04-28
• Study First Posted: 2015-04-29
• Primary Completion: 2020-06-30
• Study Completion: 2020-06-30
• Status Verified: 2020-11
• Last Update Submitted: 2020-11-11
• Last Update Posted: 2020-11-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 194

Inclusion Criteria

• females of childbearing potential experiencing reproductive endocrinology related problems

Exclusion Criteria

• male or female not of childbearing potential

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.

Trial Locations

Locations (1)

Regional One Health Ob-Gyn Clinic; 🇺🇸 Memphis, Tennessee, United States