Under construction – not a live service
Sign in
Taking people in BrazilNo phase

Compares two surgeries to lower ovarian cancer risk in high-risk women

Tests removing the fallopian tubes first, with later ovary removal, in women with gene changes.

Plain-language title generated from the registry record
Registry title: TUBectomy With Delayed Oophorectomy in High Risk Women to Assess the Safety of Prevention

Key facts

Where
São Paulo, BrazilSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 25 and 50 years old?
  • Have you ever been told you have ovarian, fallopian tube or peritoneal cancer?

Source: NCT04294927, who can take part

Where in Brazil

  • AC Camargo Cancer CentreSão Paulo, BrazilTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University Medical Center Nijmegen
Trial code
NCT04294927
Record updated
6 April 2026
Original description
The aim of the project is to evaluate the risk-reducing salpingectomy with delayed oophorectomy as an alternative for risk-reducing salpingo-oophorectomy in high risk women with respect to ovarian cancer incidence.Read full original descriptionShow less

TUBectomy With Delayed Oophorectomy as Alternative for Risk-reducing Salpingo-oophorectomy in High Risk Women to Assess the Safety of Prevention: TUBA-WISP II Study.

The aim of the project is to evaluate the risk-reducing salpingectomy with delayed oophorectomy as an alternative for risk-reducing salpingo-oophorectomy in high risk women with respect to ovarian cancer incidence.

Inclusion: Women with a class 5 (definitely pathogenic) BRCA1, BRCA2, RAD51C, RAD51D or BRIP1 germline mutation in one of the participating centers; Age at inclusion; BRCA1: 25-40 years; BRCA2: 25-45 years; RAD51C, RAD51D, BRIP1: 25-50 years; Childbearing completed; Presence of at least one fallopian tube; Participants may have a personal history of non-ovarian malignancy; Informed consent must be obtained and documented according to national and local regulatory requirements and the local rules followed in the institution.

Exclusion: Prior bilateral salpingectomy; A personal history of ovarian, fallopian tube or peritoneal cancer; Current diagnosis or treatment for malignant disease; Postmenopausal status (natural menopause or due to treatment); Wish for second stage RRO within two years after RRS; Legally incapable.

ClinicalTrials.gov NCT04294927