Characteristics of Women With Reproductive Concerns

Endocrine Disorders of Female Reproductive System Clinical Trial

Official title:

Clinical Characteristics of Women Presenting to the Reproductive Endocrinology Clinic

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02429336
• Other study ID #: 11-01368-XP
• Status: Completed
• Start date: January 2012
• Est. completion date: June 30, 2020

Study information

• Verified date: November 2020
• Source: University of Tennessee
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 194
• Est. completion date: June 30, 2020
• Est. primary completion date: June 30, 2020
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 8 Years and older

Eligibility

Inclusion Criteria:

• females of childbearing potential experiencing reproductive endocrinology related problems

Exclusion Criteria:

• male or female not of childbearing potential

Related Conditions & MeSH terms

• Endocrine Disorders of Female Reproductive System
• Endocrine System Diseases

Locations

Country	Name	City	State
United States	Regional One Health Ob-Gyn Clinic	Memphis	Tennessee

Sponsors (1)

Lead Sponsor	Collaborator
University of Tennessee

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Data collection from patients' charts.	Data collection from patients' charts.	up to 1 year from the time of signing the informed consent for data collection