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 @ 12:05 AM
Ignite Modification Date:
2025-12-25 @ 12:05 AM
NCT ID:
NCT00572858
Eligibility Criteria:
Inclusion Criteria:
* Premenopausal by WISE criteria
* English speaking (for the purposes of complete psychosocial assessment)
* Able to give informed consent
* Clinically-indicated coronary angiography within the last 24 months prior to enrollment with no interim change in symptoms, hospitalization, or events.
* Non-English speaking patients will be consented but will not undergo psychosocial assessment as part of the study.
Exclusion Criteria:
* Pregnant or intention of becoming pregnant during study period.
* Current hormonal therapy (oral contraceptives, hormone replacement therapy, designer estrogens or phytoestrogens)
* History of bilateral salpingoophorectomy
Healthy Volunteers:
False
Sex:
FEMALE
Maximum Age:
55 Years
Study:
NCT00572858
Study Brief:
Protocol Section:
NCT00572858