Actively Recruiting

Phase Not Applicable
Age: 45Years +
FEMALE
Healthy Volunteers
NCT06312124

A Study of Opportunistic Salpingectomy to Prevent Ovarian Cancer

Led by Memorial Sloan Kettering Cancer Center · Updated on 2026-01-23

266

Participants Needed

10

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to find out how many participants are interested in a surgical preventive procedure after watching an educational video. Before and after watching the video, participants will complete questionnaires in the clinic.

CONDITIONS

Official Title

A Study of Opportunistic Salpingectomy to Prevent Ovarian Cancer

Who Can Participate

Age: 45Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 45 years or older
  • Scheduled visit with a nongynecologic surgeon
  • Female or assigned female at birth
  • At least one in situ fallopian tube
  • No desire or plan to have children in the future
  • Average risk of developing ovarian cancer (no known genetic risk factors)
  • Planned nongynecologic, intraabdominal, or pelvic surgery
  • Considered suitable candidate by gynecologic and nongynecologic surgeons
  • Approved and signed informed consent
Not Eligible

You will not qualify if you...

  • Not fluent in English or Spanish (except for strong candidates eligible for Part 2 without Part 1)
  • Known inherited ovarian cancer susceptibility
  • Personal history of gynecologic malignancy
  • Carrier of hereditary breast or ovarian cancer gene variants (e.g., BRCA1, BRCA2)
  • Suspicious ovarian, fallopian tube, or uterine lesion on preoperative imaging
  • Previous bilateral salpingectomy or bilateral salpingo-oophorectomy
  • Presence of tubal-implanted birth control devices (e.g., ESSURE) at surgery time
  • Current pregnancy
  • Emergency procedures requiring consent in inpatient setting or life-threatening situations
  • Anticipated significant surgical time increase (>30-40 minutes) due to OS
  • Inability to access pelvis during planned procedure
  • Known pelvic fibrosis or significant adhesions
  • Procedures performed with palliative intent only

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 10 locations

1

Johns Hopkins University (Data Collection Only)

Baltimore, Maryland, United States, 21287

Actively Recruiting

2

Dana Farber Cancer Institute (Data Collection Only)

Boston, Massachusetts, United States, 02115

Not Yet Recruiting

3

Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities)

Basking Ridge, New Jersey, United States, 07920

Actively Recruiting

4

Memorial Sloan Kettering Monmouth (Limited protocol activities)

Middletown, New Jersey, United States, 07748

Actively Recruiting

5

Memorial Sloan Kettering Bergen (Limited Protocol Activities)

Montvale, New Jersey, United States, 07645

Actively Recruiting

6

Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (Limited protocol activities)

Commack, New York, United States, 11725

Actively Recruiting

7

Memorial Sloan Kettering Westchester (Limited Protocol Activities)

Harrison, New York, United States, 10604

Actively Recruiting

8

Memorial Sloan Kettering Cancer Center (All Protocol Activities)

New York, New York, United States, 10065

Actively Recruiting

9

Memorial Sloan Kettering Nassau (Limited Protocol Activities)

Uniondale, New York, United States, 11553

Actively Recruiting

10

MD Anderson Cancer Center (Data Collection Only)

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

K

Kara Long Roche, MD

CONTACT

M

Martin Weiser, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SEQUENTIAL

Primary Purpose

PREVENTION

Number of Arms

1

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