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The ''CORE-64'' Study.

Completed
Conditions
Multicenter, clinical study.
Registration Number
NL-OMON21519
Lead Sponsor
Toshiba Medical Systems Corporation
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
6
Inclusion Criteria

1. Male or female patients;

2. age 40 years or greater;

Exclusion Criteria

1. Known allergy to iodinated contrast media;

2. history of contrast-induced nephropathy;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sensitivity and specificity of MDCTA for identifying coronary artery stenosis ¡Ý 50% in a patient with suspected coronary artery disease, compared with conventional coronary angiography.
Secondary Outcome Measures
NameTimeMethod
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