Ovarian Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Women who carry a change (variant) in the BRCA1 or BRCA2 gene, including those with changes in both genes, or those with a gene change whose meaning is not yet fully understood (called a "variant of uncertain significance")
- Women who have already received genetic counseling at any medical facility before joining the study
- Women who are 20 years of age or older
- Women who are willing and able to give written consent to take part
Who may not be able to join:
- Women who have been diagnosed with ovarian cancer or fallopian tube cancer at the time they are asked to join the study (confirm with trial site)
- Women who have previously been diagnosed with ovarian cancer, fallopian tube cancer, or peritoneal (abdominal lining) cancer — note that having a personal history of breast cancer does not automatically exclude someone (confirm with trial site)
- Women who the study doctor considers unsuitable for the study for any other reason
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Akira Hirasawa, M.D., Ph.D., Okayama University
Phone: +81-86-235-7436
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Occurrence of ovarian, fallopian tube, and peritoneal carcinoma
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.