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FFRct versus SPECT for Cardiovascular Abnormalities (AFFECTS Trial)
Phase 3
Waitlist Available
Led By David Brown, MD
Research Sponsored by Baylor Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights
AFFECTS Trial Summary
This study is evaluating whether a new test can help determine if a person has significant coronary artery disease.
AFFECTS Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Positive finding of hemodynamically significant CAD according to FFRct.
Positive finding of hemodynamically significant CAD according to ICA +/- iFFR.
Positive finding of hemodynamically significant CAD according to SPECT.
Secondary outcome measures
Cumulative radiation exposure in the study cohort during SPECT, cCTA, and ICA and potential impact of FFRct in reducing radiation exposure in patients with no hemodynamically significant CAD.
Physician intuition regarding presence of vessel-specific, hemodynamically significant CAD after review of FFRct results.
Potential economic impact of FFRct in decreasing referral to ICA in patients without hemodynamically significant CAD.
AFFECTS Trial Design
1Treatment groups
Experimental Treatment
Group I: FFRct versus SPECTExperimental Treatment1 Intervention
Comparison of the diagnostic performance of FFRct and SPECT in subjects with suspected stable CAD
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Who is running the clinical trial?
Baylor Research InstituteLead Sponsor
200 Previous Clinical Trials
202,956 Total Patients Enrolled
David Brown, MDPrincipal InvestigatorBaylor Research Institute
4 Previous Clinical Trials
489 Total Patients Enrolled
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