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:
2025-12-24 @ 7:43 PM
Ignite Modification Date:
2025-12-24 @ 7:43 PM
NCT ID:
NCT00508703
Eligibility Criteria:
Inclusion Criteria:
1. Patients who have been treated with a hysterectomy for carcinoma of the uterine cervix or endometrium who require post-operative radiation or chemoradiation therapy because of positive pelvic lymph nodes or other high-risk local findings.
2. Patients must have no evidence of metastatic disease outside of the pelvis.
3. Patients must have a Karnofsky Performance Status of \>60.
4. The patient must be able to understand the protocol and sign a study-specific informed consent. .
Exclusion Criteria:
1. Karnofsky Performance Status \< 60.
2. Patients with para-aortic nodal disease or who require extended field radiotherapy beyond the pelvis.
3. Obese patients who exceed the size limits of hte treatment table or CT scanner.
4. Mental status changes or bladder control problems that make the patient unable to comply with bladder-filling instructions.
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00508703
Study Brief:
Protocol Section:
NCT00508703