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 @ 12:22 AM
Ignite Modification Date:
2025-12-25 @ 12:22 AM
NCT ID:
NCT00579358
Eligibility Criteria:
Inclusion Criteria:
* Adults and children (both parent's signature required) who are able to give informed consent
* Adults or children who are prior diagnosed with congenital heart disease and/or who has immediate family member(s) with congenital heart disease (immediate family members include: subject's parents, siblings, and subject's children)
* If subject is the only one affected and subject does not disclose of any family member being affected, than only subject will be enrolled
* If subject is affected and disclose that a family member is affected, that family member will be contacted (with permission) to participate in the study
* Patients of all ethnical origin
Exclusion Criteria:
* Patients diagnosed with no congenital heart disease (as determined by their medical assessment); (if subjects who are unaffected disclose that a family member is affected, with permission, that family will be contacted for participation)
* Patients who are unable to provide informed consent/assent
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT00579358
Study Brief:
Protocol Section:
NCT00579358