Ovarian Cancer Trial, Recruiting NCT05287451 Sponsor: M.D. Anderson Cancer Center Condition: Ovarian Cancer
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Ovarian Cancer Trial, Recruiting

NCT05287451
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
10 May 2022
Est. completion
26 December 2026

Where this trial is recruiting

🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov