Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:19 PM
Ignite Modification Date:
2026-03-26 @ 3:19 PM
NCT ID:
NCT07382505
Eligibility Criteria:
Inclusion Criteria:
* Histologically confirmed endometrial cancer or cervical cancer.
* Scheduled for or completed standard treatment (Surgery, Adjuvant therapy, or CCRT).
* Provision of written informed consent for study participation and biospecimen collection
Exclusion Criteria:
* Synchronous other malignancies (cancer requiring treatment within the last 5 years).
* Persistent infection or bleeding tendency that makes repeated blood collection unsafe.
* Inability to follow-up or communicate (e.g., due to geographic or cognitive reasons).
* Any condition that the principal investigator deems inappropriate for the study.
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT07382505
Study Brief:
Protocol Section:
NCT07382505