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NCT06312124Recruiting

A Study of Opportunistic Salpingectomy to Prevent Ovarian Cancer

A Multi-Disciplinary Approach to the Opportunistic Salpingectomy for Primary Prevention of Ovarian Cancer

Source: ClinicalTrials.gov · Last updated 24 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
266 (estimated)
First submitted
8 Mar 2024
Start date
8 Mar 2024
Primary completion date
8 Mar 2028
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT06312124

What you commit to

  • Study type: Interventional
  • Planned participants: 266
  • From 8 Mar 2024 to the primary completion date, 8 Mar 2028
  • 10 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous bilateral salpingectomy or bilateral salpingo-oophorectomy
  • Presence of ESSURE, or other tubal-implanted birth control at the time of surgery

Other illness

  • Known inherited ovarian cancer susceptibility
    • Part II
  • Personal history of a gynecologic malignancy
  • Carrier of a hereditary breast or ovarian cancer variant (e.g., BRCA1, BRCA2, BRIP1, PALB2, RAD51C, RAD51D, MLH1, MSH2, MSH6, PMS2)
  • Emergent procedure or emergency procedure that has to be completed within 24 hours where clinical consent occurs in the inpatient setting or where the patient's immediate well-being is in danger or condition may be life threatening
  • Known history of pelvic fibrosis or significant adhesions.

Other

  • Part I
  • Not fluent in English or Spanish
    • ° If there is a non-english or non-spanish speaking participant who is a strong candidate and meets all other criteria for Part 2, they are able to go directly onto Part 2 without completing Part 1. (Please see additional details in section 4.1 and 7.0.)
  • Suspicious ovarian, fallopian tube, or uterine lesion on preoperative imaging
  • Current pregnancy
  • Primary surgeon anticipates that OS will add significant time (\>30-40min) to the planned procedure.
  • Inability to access the pelvis (ex., patient prone/lateral position) during the planned procedure.
  • Procedures with palliative intent only

Who the study is looking for

  • Part I
  • Age ≥45 years
  • Scheduled visit with a nongynecologic surgeon
  • Female or assigned female at birth
    • Part II
  • Age ≥45 years
  • At least one in situ fallopian tube
  • No desire or plan to have children in the future
  • Average risk of developing ovarian cancer
    • ° Note: Average risk patients are defined as patients with no known genetic risk factor for developing ovarian cancer. Patients who, after obtaining family history, are suspected to have a hereditary ovarian cancer syndrome but have not yet been tested, will be referred for genetic evaluation.
  • Planned nongynecologic, intraabdominal, or pelvic surgery
  • Deemed to be a suitable candidate by gynecologic surgeon and primary nongynecologic surgeon (for example, on the basis of surgical history and current malignancy status)
  • Approved and signed informed consent

Age in the registry: 45 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Johns Hopkins University (Data Collection Only)
Coordinator of this site? Confirm its status
BaltimoreUnited StatesRecruiting
Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities)
Coordinator of this site? Confirm its status
Basking RidgeUnited StatesRecruiting
Dana Farber Cancer Institute (Data Collection Only)
Coordinator of this site? Confirm its status
BostonUnited StatesNot yet recruiting
Memorial Sloan Kettering Cancer Center @ Suffolk-Commack (Limited Protocol Activities)
Coordinator of this site? Confirm its status
CommackUnited StatesRecruiting
Memorial Sloan Kettering Westchester (Limited Protocol Activities)
Coordinator of this site? Confirm its status
HarrisonUnited StatesRecruiting
MD Anderson Cancer Center (Data Collection Only)
Coordinator of this site? Confirm its status
HoustonUnited StatesRecruiting
Memorial Sloan Kettering Monmouth (Limited Protocol Activities)
Coordinator of this site? Confirm its status
MiddletownUnited StatesRecruiting
Memorial Sloan Kettering Bergen (Limited Protocol Activities)
Coordinator of this site? Confirm its status
MontvaleUnited StatesRecruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activities)
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Memorial Sloan Kettering Nassau (Limited Protocol Activities)
Coordinator of this site? Confirm its status
UniondaleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.