Regional One Health Ob-Gyn Clinic
Memphis, Tennessee, 38103, United States
NCT Number: NCT02429336
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.
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Notify Me8 year and older
Female
Observational
Memphis, Tennessee, 38103, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: up to 1 year from the time of signing the informed consent for data collection
Data collection from patients' charts.
University of Tennessee
Other
Clinical Characteristics of Women Presenting to the Reproductive Endocrinology Clinic
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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