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 have not yet reached menopause and have a confirmed harmful gene mutation in one or more of the following genes: BRCA1, BRCA2, BRIP1, RAD51C, PALB2, or RAD51D.
- Women aged 25–40 if they carry a BRCA1 mutation, aged 25–45 if they carry a BRCA2 mutation, or aged 30–50 if they carry a BRIP1, RAD51C, RAD51D, or PALB2 mutation (if multiple mutations are present, the age range is based on the BRCA mutation).
- Women who no longer need their fallopian tubes for natural pregnancy, though future plans to use IVF are acceptable.
- Women who still have at least one fallopian tube remaining.
- Women who have had a previous cancer diagnosis, as long as it was not ovarian, fallopian tube, or peritoneal cancer.
- Women who have given their informed written consent to participate.
Who may not be able to join:
- Women who have gone through menopause, either naturally or as a result of cancer treatment (defined as having had no periods for 12 months without another medical explanation).
- Women who already plan to have a full removal of their ovaries and fallopian tubes within two years of joining the trial, if that plan is clear at the time of enrollment.
- Women who are not legally able to consent for themselves.
- Women who have already had both fallopian tubes surgically removed.
- Women who have a personal history of ovarian, fallopian tube, or peritoneal cancer.
- Women who currently have signs of, a diagnosis of, or are receiving treatment for an active cancer (note: certain hormone-related medications such as Tamoxifen, Aromatase Inhibitors, and SERMs are permitted — confirm with trial site).
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: Roni Wilke, MD, M.D. Anderson Cancer Center
Phone: (713) 822-4502
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
To evaluate the non-inferiority of the innovative treatment (RRS with delayed RRO) as compared to the standard treatment (RRSO) with respect to high grade serous (ovarian) cancer incidence in BRCA1/2 gene germline mutation carriers.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.