Characterization of Changes in Ventricular Mechanics in Response to Lexiscan Stress Using Tagged Cine Cardiac Magnetic Resonance Imaging
Completed · Phase 4
Conditions studied: Coronary Artery Disease
In brief
The purpose of this study is to measure the changes in cardiac function during a Lexiscan pharmacologic stress test using cardiac magnetic resonance imaging test.
Key facts
- Study ID
- NCT02115308
- Run by
- Timothy M. Bateman
- People needed
- 40
- Starts
- 2014-09-03
- Expected to finish
- 2018-03-23
- Last updated by the study team
- 2018-09-19
Who can join
Age: 19 and older, up to 90. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Myocardial rest/regadenoson stress perfusion PET study within 60 days
- Normal rest LVEF (greater than or equal to 50%)
- No change in symptoms or treatment between the PET and the MRI study
- Willing to consent to the study
- Male or female who is either post-menopausal, surgically sterile, or if has a childbearing potential, a negative pregnancy test within 2 days prior to the MRI study.
You may not qualify if…
- Renal dysfunction (estimated glomerular filtration rate < 60 mL/min/1.73m2) within 6 months
- Metallic implants, pacemaker, blood vessel clip (contra-indicated for MRI)
- Patient size exceeds MRI bore/table limits: (Max body diameter > 60 cm, weight > 136 kg)
- History of gadolinium contrast allergy or intolerance
- Second or third degree AV block
- Sinus node dysfunction
- Acute myocardial infarction (past 3 months)
- Actively wheezing or with acute asthma or bronchospastic attacks requiring changes in therapy within the past 30 days
- Patients that have experienced a previous hypersensitivity reaction thought to be related to regadenoson
Where it is running
- Saint Luke's Health System — Kansas City, Missouri, United States
Full record on ClinicalTrials.gov
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