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:
2025-12-25 @ 2:28 AM
Ignite Modification Date:
2025-12-25 @ 2:28 AM
NCT ID:
NCT03466034
Eligibility Criteria:
Inclusion Criteria:
1. ≥18 years of age on the day of signing the informed consent.
2. Histologically confirmed endometroid or serous endometrial cancer.
3. Scheduled to have hysterectomy at the cancer centre
4. Identifiable tumour mass on staging MRI.
5. Voluntarily agreed to participate by giving written informed consent.
Exclusion Criteria:
1. Life expectancy of \< 6 months.
2. Ferromagnetic implants, contraindicating MRI
3. Claustrophobia so unable to tolerate MRI
4. Unable to lie flat
5. Ascites sufficient to prevent patient being fitted in the scanner bore
6. Histology unlikely to show variation in TP53 status, or heavily calcified disease.
7. Radiotherapy to the abdomen or pelvis within 6 months of the screening visit.
8. Unresolved bowel obstruction.
9. Currently participating or has participated in a study with an investigational compound or device within 30 days of the start of treatment.
10. History or current evidence of any condition, therapy, or lab abnormality that might confound the results of the study, interfere with patient's participation for the full duration of the study, or is not in the best interest of the patient to participate.
11. Unlikely to comply with the requirements of the study.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03466034
Study Brief:
Protocol Section:
NCT03466034