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A single-center, prospective cohort study of monitoring, management and intervention in patients at high risk for ovarian, fallopian tube, or peritoneal cancer

A single-center, prospective cohort study of monitoring, management and intervention in patients at high risk for ovarian, fallopian tube, or peritoneal cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062438
Enrollment
Unknown
Registered
2022-08-07
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ovarian cancer

Interventions

RRSO group:Risk-reducing salpingo-oophorectomy
RRESDO group:Risk-reducing salpingectomy and delayed oophorectomy
Non-surgical intervention group:No

Sponsors

The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. People with high risk of genetic brCA1/2, BRIP1, RAD51C and RAD51D gene mutations or hereditary family history of ovarian cancer or hereditary family history of breast, ovarian and pancreatic cancer; 2. Having or not having children; 3. Age >=40 years (according to NCCN guidelines, patients with BRCA1 gene mutation can undergo prophylactic surgery until they are 35~40 years old after childbirth or insist on it); 4. The population with a family history of hereditary breast cancer, ovarian cancer and pancreatic cancer should be at least 35 years old, combined with the age of diagnosis of the first episode in the family; 5. Patients with breast cancer who are recommended by breast surgeons or oncologists for surgical castration after surgery; 6. Sign informed consent and complete the questionnaire.

Exclusion criteria

Exclusion criteria: 1. Auxiliary examination such as B-ultrasound or other imaging suggested the possibility of malignant tumor; 2. combined with other active malignant tumors except breast cancer; 3. Patients who are unwilling to sign or withdraw informed consent; 4. It is not suitable for inclusion in this study as determined by the researcher.

Design outcomes

Primary

MeasureTime frame
CA125;HE4;Imaging manifestation;Ovarian function test;

Countries

China

Contacts

Public ContactZhou Ying

The First Affiliated Hospital of University of Science and Technology of China

caddiezy@ustc.edu.cn+86 13865901025

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026