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 @ 4:11 AM
Ignite Modification Date:
2025-12-25 @ 4:11 AM
NCT ID:
NCT02088320
Eligibility Criteria:
Inclusion Criteria:
1. Male or female sex, age \>18 years who are having an echocardiogram done for clinical reasons. Based on the potential for further support of our work, this may expand to include volunteers who would otherwise not be undergoing an echocardiogram.
2. Negative pregnancy test for women of childbearing potential
3. If eligible for cMRI, estimated glomerular filtration rate (eGFR) of \> 30 mL/min
4. If eligible for cMRI, cMRI checklist obtained
5. Able to give informed consent
Exclusion Criteria:
1. Unable to give informed consent
2. Known right-to-left, bidirectional, or transient right-to-left cardiac shunts
3. Currently participating in another clinical treatment trial
4. Known allergic reaction to Optison ultrasound contrast
5. If eligible for cMRI, known allergic reaction to cMRI contrast
6. If eligible for cMRI, contraindication to cMRI
7. If eligible for cMRI, pre-cMRI eGFR \< 30 mL/min
8. Pregnancy/Nursing
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02088320
Study Brief:
Protocol Section:
NCT02088320