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NCT07502586 · ClinicalTrials.gov registry record

Turner Syndrome: Genetic Considerations

A clinical trial, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

Recruiting
Registry status
500
Enrollment target

NCT07502586: Recruiting study, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

NCT07502586 is a clinical trial that is actively recruiting participants, run by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The registered enrollment target is 500 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07502586 is actively recruiting participants, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

RECRUITING
Registry status
500 participants
Enrollment target

Study Summary

Background: Turner syndrome (TS) is a rare genetic condition. It happens when a person is born missing all or part of an X sex chromosome. People with TS can have heart defects, short stature, autoimmune conditions, and malformations. Many women with TS never have periods and cannot conceive; however, some women have normal ovaries (egg cells). Researchers want to learn more about why some women with TS are fertile and others are not. To do this, they need to be able to compare the genes of many women who have TS. Objective: To create a genetic database of people with TS. Eligibility: People of any age with TS. Biological parents and other relatives are also needed. Design: Participants who agree to join this study will be asked to enroll in a second study; that study is called NIAID Centralized Sequencing Protocol (Protocol No. 17I0122). Participants will have 1 study visit. They may fill out a survey or do an interview. They will provide blood, saliva, or other tissue samples. Those samples will be used for genetic tests. The visit will take 1 hour. The information collected in those tests will be collected for use in the database created as part of this study.

Primary Outcome

To create a database which will allow for evaluation of patient with turner syndrome and their family member

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2026-03-24
Est. Completion 2028-08-31

What NCT07502586 shows while recruiting

NCT07502586 is an observational study that tracks outcomes without assigning an intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT07502586 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07502586 about?

NCT07502586 is a clinical study titled "Turner Syndrome: Genetic Considerations". Background: Turner syndrome (TS) is a rare genetic condition. It happens when a person is born missing all or part of an X sex chromosome. People with TS can have heart defects, short stature, autoimmune conditions, and malformations. Many women with TS never have periods and cannot conceive; howev...

What is the current status of trial NCT07502586?

This trial is currently recruiting. The enrollment target is 500 participants. The study started on 2026-03-24. Estimated completion is 2028-08-31.

Who is sponsoring clinical trial NCT07502586?

This trial is sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT07502586, the US trial registry maintained by the National Library of Medicine. NCT07502586 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.