Hunt for thyroid cancer genes begins in 1,200 families
NCT ID NCT02776969
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study aims to find the genetic changes that make some families more likely to develop papillary thyroid cancer. Researchers will analyze DNA from 1,200 people who either have this cancer and have at least three affected relatives, or are family members of such patients. The goal is to identify specific gene variants linked to inherited risk, which could lead to better screening and understanding of the disease.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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Locations
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Ohio State University Comprehensive Cancer Center
Columbus, Ohio, 43210, United States