Endocrine Disorders of Female Reproductive System
Conditions
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.
Interventions
None listed
Sponsors
University of Tennessee
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
FEMALE
Age
8 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* females of childbearing potential experiencing reproductive endocrinology related problems
Exclusion criteria
* male or female not of childbearing potential
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 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. |
Countries
United States
Outcome results
None listed