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Clinical Trials/NL-OMON33255
NL-OMON33255
Completed
Not Applicable

A Multi-Center Study Combined Non-Invasive Coronary Angiography and Myocardial Perfusion Imaging Using 320 Detector Computed Tomography - Coronary Angiography and Myocardial Perfusion with 320 Detector CT

Toshiba Medical Systems0 sites20 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Stenoses
Sponsor
Toshiba Medical Systems
Enrollment
20
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Sponsor
Toshiba Medical Systems

Eligibility Criteria

Inclusion Criteria

  • Male or female patients, age 45\-85\. ;Suspected or diagnosed coronary artery disease with a clinical indication for coronary angiography; and planned coronary angiography within the next 60 days.;Able to understand and willing to sign the Informed Consent Form.

Exclusion Criteria

  • Known allergy to iodinated contrast media;History of contrast\-induced nephropathy;History of multiple myeloma or previous organ transplantation;Elevated serum creatinine OR calculated creatinine clearance of \<60 ml/min;Atrial fibrillation or uncontrolled tachyarrhythmia, or advanced atrioventricular block (second or third degree heart block);Evidence of severe symptomatic heart failure (NYHA Class III or IV); Known or suspected moderate or severe aortic stenosis ;Previous cardiac surgery;Coronary artery intervention within the last 6 months ;Known or suspected intolerance or contraindication to beta\-blockers including;Severe pulmonary disease (chronic obstructive pulmonary disease)

Outcomes

Primary Outcomes

Not specified

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