An observational study in Endocrine Disorders of Female Reproductive System, sponsored by University of Tennessee. Completed at 1 site in United States. Open to female participants aged 8 Years and older. Per ClinicalTrials.gov, last updated 2020-11-13.
Sponsored by University of Tennessee · Observational
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.
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.
307 studies on the registry are indexed under Endocrine System Diseases; 52 are open to participants now.
This study's enrollment of 194 is close to the median of 200 across 84 observational studies indexed under Endocrine System Diseases.
Browse Endocrine System Diseases studies →University of Tennessee is the lead sponsor of 139 studies on the registry; 21 are open to participants now.
Of its 7 completed or terminated interventional studies of FDA-regulated products, 2 (29%) have results posted.
Counted across the registry records on this site, refreshed daily.
Population: All patients presenting to the reproductive endocrinology clinic.
Exclusion Criteria:
Data collection from patients' charts.
Data collection from patients' charts.
Time frame: up to 1 year from the time of signing the informed consent for data collection
This study is completed, as verified in Nov 2020. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.
University of Tennessee