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Clinical Trials/NCT02429336
NCT02429336
Completed
Not Applicable

Clinical Characteristics of Women Presenting to the Reproductive Endocrinology Clinic

University of Tennessee1 site in 1 country194 target enrollmentJanuary 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Endocrine Disorders of Female Reproductive System
Sponsor
University of Tennessee
Enrollment
194
Locations
1
Primary Endpoint
Data collection from patients' charts.
Status
Completed
Last Updated
5 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
June 30, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • females of childbearing potential experiencing reproductive endocrinology related problems

Exclusion Criteria

  • male or female not of childbearing potential

Outcomes

Primary Outcomes

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.

Study Sites (1)

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