A Cohort Study of Uterine Malignancies
- Conditions
- Cervical CancerEndometrial Cancer
- Registration Number
- NCT05635123
- Brief Summary
The purposes of current study were to explore the relationship between cervical cancer/endometrial cancer and demographic information, behavior and life style, pregnancy-related factors, and disease history, and to study the factors affecting the prognosis of cancers. In addition, omics tests were performed on the biological specimens to identify the diagnostic markers and prognostic biomarkers.
- Detailed Description
After being informed about the study and potential risks, all patients who meet the eligibility requirements will be enrolled.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 6200
- Age 20-75 years;
- Women with cervical cancer or endometrial cancer with a definite pathological diagnosis for the first time;
- Women attending a health check-up;
- Obtain informed consent and sign an informed consent form.
- Patients who are unable to cooperate with the investigations such as mental disorders or cognitive impairment;
- Patients with cancer other than cervical cancer or endometrial cancer;
- Women who have received hysterectomy or pelvic radiation therapy previously.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method progression free survival (PFS) 60 months progression free survival for patients with cervical cancer or endometrial cancer
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Women's hospital school of medicine zhejiang university
🇨🇳Hangzhou, Zhejiang, China