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Neuro-Cardio Study
Protocol: STUDY00003379
Full Title
Use of Cerebrotech VISOR to Detect Ischemic Changes in the Brain during Cardio-cerebrovascular Procedures
Description
We are enrolling people who are undergoing a cardiac neurological procedure. The purpose of this study is to collect information from a medical device used in these procedures called the VISOR device. We will collect information before and after a person has a cardio-cerebrovascular procedure to see how well the device detects neurological injury from the procedure.

The information we collect for this study is already being collected in your medical record as part of your care. You will be in this study for about 3 months. You will not be asked to do anything additional as a result of being in this study. This study takes place at Gates Vascular Institute, 875 Ellicott St, Buffalo, NY 14203.

Compensation is not available. Please contact Ammad Baig (716-986-0545 or abaig@ubns.com) for more information about this study.
Compensation: No
Eligibility
-Adults ages 18+.
-Undergoing cardiovascular procedures including trans-aortic valve replacement (TAVR), left atrial appendage closure, electrophysiological ablation, coronary artery bypass grafting (CABG) and valve replacement surgery, with the application of Cerebrotech VISOR.
Age Group: Adults
Principal Investigator: ADNAN SIDDIQUI
Contact(s)
ELIZABETH SHISLER
emczosek@buffalo.edu
+1 716-929-9681
Want to Learn More?

Let us know how the study team can reach you. If you do not hear back within 2 business days, reach out to the study team directly at the contact information above or email ctsiresearch@buffalo.edu and someone will assist you.

Your information will be shared only with the research study team for recruitment purposes and designated CTSI personnel for project quality assurance and will remain confidential. Your information will be stored indefinitely. Should you no longer want this information to be provided in the aforementioned ways, please contact ctsiresearch@buffalo.edu.