Uterine Lavage to Detect Ovarian Cancer Risk

Part of paid clinical trials in Seattle, Washington.

Sponsor
University of Washington
Study ID
NCT07772869
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • BRCA Hereditary Ovarian Carcinoma
  • Fallopian Tube High Grade Serous Adenocarcinoma
  • Ovarian High Grade Serous Adenocarcinoma
  • Primary Peritoneal High Grade Serous Adenocarcinoma

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Uterine Lavage — OTHER
    Undergo uterine lavage
  • Archive Sample — PROCEDURE
    Ancillary studies
  • Survey Administration — OTHER
    Ancillary studies

Study Details

This clinical trial develops a non-surgical approach using uterine lavage samples to screen for progression to ovarian cancer in high-risk patients carrying BRCA mutations. Women with inherited mutations in the BRCA1 and BRCA2 genes (BRCA carriers) have a much higher lifetime risk of developing ovarian cancer. Currently there are no effective ovarian cancer screening or early detection tests for BRCA carriers. Uterine lavage is a procedure that uses saline to rinse and collect cells from the fallopian tube. Molecular analysis of these samples may help proactively detect genetic alterations that are indicative of progression to ovarian cancer in women with BRCA mutations.

Key Dates

First listed
Aug 19, 2026
Start date
Aug 31, 2026
Status verified
Aug 2026
Primary completion
Jun 1, 2028
Completion
Jun 1, 2028

Study Design

Enrollment
75 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING

Arms

  • Experimental: Screening (uterine lavage)
    Patients undergo uterine lavage prior to their standard of care risk-reduction surgery and uterine lavage samples undergo molecular analysis on study.

Primary Outcome Measure

TP53 mutation burden (MB) [ Time Frame: Up to 2 years ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Fred Hutch/University of Washington Cancer ConsortiumSeattleWashington98109
Intake Coordinators
206-616-3913
Intake Coordinators
206-221-6648
Barbara Norquist, MD (PRINCIPAL_INVESTIGATOR)

Find similar trials in Seattle, WA

Related Studies