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 @ 2:54 AM
Ignite Modification Date:
2025-12-25 @ 2:54 AM
NCT ID:
NCT00196833
Eligibility Criteria:
Inclusion Criteria:
* Cohort 1: Women with histologically confirmed breast cancer during pregnancy
* Cohort 2: Patients ≤ 40 years with histological confirmed breast cancer who are not pregnant (patients who have been pregnant recently can also be collected into this cohort)
* Informed consent for data collection (for prospective participants) and biomaterial collection. For retrospective participants an informed consent is not required as long as the data are anonymously captured
Exclusion Criteria:
* Cohort 1: Diagnosis of breast cancer outside the period of pregnancy
* Cohort 2: Age at diagnosis of breast cancer \> 40 years
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00196833
Study Brief:
Protocol Section:
NCT00196833