NCT02429336

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
194

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2012

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2012

Completed
3.2 years until next milestone

First Submitted

Initial submission to the registry

March 23, 2015

Completed
1 month until next milestone

First Posted

Study publicly available on registry

April 29, 2015

Completed
5.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2020

Completed
Last Updated

November 13, 2020

Status Verified

November 1, 2020

Enrollment Period

8.5 years

First QC Date

March 23, 2015

Last Update Submit

November 11, 2020

Conditions

Endocrine Disorders of Female Reproductive System

Outcome Measures

Primary Outcomes (1)

  • Data collection from patients' charts.

    Data collection from patients' charts.

    up to 1 year from the time of signing the informed consent for data collection

Eligibility Criteria

Age8 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Population: All patients presenting to the reproductive endocrinology clinic.

You may qualify if:

  • females of childbearing potential experiencing reproductive endocrinology related problems

You may not qualify if:

  • male or female not of childbearing potential

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Regional One Health Ob-Gyn Clinic

Memphis, Tennessee, 38103, United States

Location

Study Officials

  • Laura Detti, M.D.

    Associate Professor, UTennessee Health Science Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 23, 2015

First Posted

April 29, 2015

Study Start

January 1, 2012

Primary Completion

June 30, 2020

Study Completion

June 30, 2020

Last Updated

November 13, 2020

Record last verified: 2020-11

Locations

US(1)