a cohort study of young female cancer survivors who received fertility-sparing treatment
- Conditions
- Neoplasms
- Registration Number
- KCT0009578
- Lead Sponsor
- Koera University Guro Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 200
1)Women diagnosed with female cancer (ovarian cancer, uterine cancer, cervical cancer)
-Including ovarian borderline tumors, endometrial epithelium tumors
2)a woman under the age of 45
3)Cancer survivors who have received fertility preservation treatment and have been treated
4)Cancer Survivors More Than 3 Months After Diagnosis
1)No fertility preservation treatment
- Removal of uterus or removal of both ovaries due to surgery
-Early menopause due to anticancer or radiation therapy, loss of uterine function
2)Ovarian cancer, uterine cancer, cervical cancer and other female cancer
Q: Breast cancer
3)If you are diagnosed with ovarian cancer, uterine cancer, cervical cancer, and other carcinomas and require additional treatment
4)If you already have a diagnosed sexual dysfunction prior to cancer treatment
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Identifying the occurrence of sexual dysfunction and unmet needs after treatment in young female cancer survivors who received fertility preservation treatment
- Secondary Outcome Measures
Name Time Method Comparison of risk factors related to recurrence risk after fertility preservation treatment and effectiveness between fertility preservation treatments, identification of unmet needs. Confirmation of menopause, pregnancy, and fertility rates and identification of unmet needs after fertility preservation cancer treatment. Confirmation of deterioration of quality of life after childbearing preservation cancer treatment and identification of unmet needs