Characteristics of Women With Reproductive Concerns
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT02429336|
Recruitment Status : Recruiting
First Posted : April 29, 2015
Last Update Posted : October 26, 2017
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.
|Condition or disease|
|Endocrine Disorders of Female Reproductive System|
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.
|Study Type :||Observational|
|Estimated Enrollment :||200 participants|
|Official Title:||Clinical Characteristics of Women Presenting to the Reproductive Endocrinology Clinic|
|Study Start Date :||January 2012|
|Estimated Primary Completion Date :||August 2020|
|Estimated Study Completion Date :||August 2022|
- 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.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02429336
|Contact: Laura Detti, M.D.||email@example.com|
|Contact: Annette B. Hickerson, RNfirstname.lastname@example.org|
|United States, Tennessee|
|Regional One Health Ob-Gyn Clinic||Recruiting|
|Memphis, Tennessee, United States, 38103|
|Contact: Annette B. Hickerson, R.N. 901-448-4784 email@example.com|
|Sub-Investigator: Ana Tobiasz, M.D.|
|Sub-Investigator: Shelby Osborne, M.D.|
|Principal Investigator:||Laura Detti, M.D.||Associate Professor, UTennessee Health Science Center|