UTHealth Turner Syndrome Research Registry
This study is creating a registry to better understand Turner Syndrome (TS), a genetic condition affecting women. Researchers are collecting genetic information from women with TS to learn why some develop heart problems like bicuspid aortic valve (BAV) or thoracic aortic aneurysm. They will compare the genetic makeup of women with TS who have these heart conditions to those who don't. The goal is to identify genetic factors that put women with TS at higher risk for heart complications. This information could help doctors better monitor and care for women with TS in the future. The study plans to enroll 200 women with a diagnosis of Turner Syndrome.
- Study design
- This is an observational study, meaning researchers will collect information without giving any new treatments. It aims to enroll 200 women.
- What's involved
- You would provide blood and/or saliva samples after giving informed consent. Researchers will use these samples for genetic tests.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary endpoint, bicuspid aortic valve and thoracic aortic aneurysm, will be measured at 10 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
UTHealth Turner Syndrome Research Registry
At a glance
Conditions
NCT03185702
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
University of Texas Health Science Center Houston
Houston, Texasstudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
Exclusion
What this trial measures
- Bicuspid aortic valve and thoracic aortic aneurysm10 years
Imaging data