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Hospital","Cincinnati","Ohio","45219",{"type":46,"coordinates":117},[118,119],-84.51439,39.12711,{"lat":119,"lon":118},[122],{"name":123,"role":54,"phone":10,"phoneExt":10,"email":10},"Jarrod Frizzell, MD",{"type":125,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100463243","physio-anatomy-clinical-data-collection-study-100463243",false,"NCT05312164","Physio-Anatomy Clinical Data Collection Study","Inclusion Criteria:\n\n* Patients \\>18 years of age.\n* Patients provide written informed consent.\n* Clinical presentation consistent with suspected coronary disease.\n* Patients who are candidates for PCI and scheduled for coronary diagnostics in the cardiac catheter lab with the intent to perform a physiological assessment for de novo lesions with stenosis, if clinically indicated.\n\nExclusion Criteria:\n\n* Presence of acute ST Elevation Myocardial Infarction (STEMI) at the time of the cath lab procedure.\n* Contraindication for FFR examination or administration of vasodilators.\n* Bacteremia or sepsis.\n* Major coagulation system abnormalities.\n* Severe hemodynamic instability or shock.\n* Heart Failure NYHA Class IV.\n* Severe valvular heart disease.\n* Prior heart transplant.\n* Acute renal failure based on diagnostic practice of the treating physician at time of screening.\n* Patient is pregnant.\n* Patient is currently enrolled in another clinical study that may impact the results of this study.\n* Patient has other co-morbid condition(s) that, in the opinion of the Investigator, could limit their","ALL","18 Years",{"count":135,"type":136},150,"ESTIMATED","OBSERVATIONAL","This is an on-label clinical study design intended for the collection of three different types of interventional procedural data using FDA-cleared cardiac catheterization technologies and drugs, each used according to its product labeling and standard practice of medicine.",[140],"Coronary 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