Plain-English translation of NCT06564428 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Ovarian Neoplasms research guide →This is a research study that collects information from patients with ovarian cancer to better understand which genetic changes run in families and increase cancer risk. Researchers will study your medical history, family background, and genetic test results to build a tool that can predict who is at highest risk for ovarian cancer. This information may help doctors decide who needs extra monitoring or preventive care.
About 10–20% of ovarian cancers are hereditary, meaning they run in families due to inherited genetic changes. In China, doctors do not yet have a good tool to predict who is at highest risk, and some families have cancer but no known genetic cause. This study aims to fill that gap so doctors can better identify and help at-risk patients.
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You would be part of a long-term study where researchers collect your medical records, family history, and results from genetic tests. You may be asked to provide a blood or tissue sample if you haven't already had genetic testing. The research team will follow your health over time and use your information to help build a risk prediction tool that could guide treatment and prevention strategies for others at high risk.
AI-generated summary from trial data · Jul 18, 2026 · Not medical advice
China