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Comparing Angiography: Multislice CT Versus Invasive Heart Catheterization (CACTI)

Primary Purpose

Coronary Arteriosclerosis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MS-CT Coronary Angiography
Sponsored by
University of Wisconsin, Madison
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Coronary Arteriosclerosis focused on measuring coronary artery disease, cardiac catheterization, CT coronary angiography, coronary angiography

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subjects >18 years old with stable clinical symptoms who are scheduled for outpatient cardiac catheterization. Able to provide written informed consent in accordance with the IRB. Exclusion Criteria: Symptoms of unstable angina/acute coronary syndrome Known allergy or adverse reaction to CT radiocontrast and/or iodine. Known absolute contraindication to Metoprolol. Significant kidney disease including creatinine > 1.5 mg/dL or GFR < 60 ml/min. Inability to breath-hold for up to 30 seconds. Women who are Pregnant or Nursing Atrial Fibrillation or any other arrhythmia that makes attaining a regular slow rhythm unlikely. History of previous stent placement or coronary bypass surgery.

Sites / Locations

  • University of Wisconsin

Outcomes

Primary Outcome Measures

The primary endpoint of the study is the ability of CTA to detect coronary disease of greater than 50% diameter stenosis (sensitivity, specificity, positive and negative predictive value) analyzed on a subject basis.

Secondary Outcome Measures

Assess CTA performance on both a vessel and coronary segment basis
Estimate the impact of coronary calcium score on ability to assess for coronary disease
Evaluate impact of scan quality of CTA performance measures

Full Information

First Posted
January 27, 2006
Last Updated
August 28, 2012
Sponsor
University of Wisconsin, Madison
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1. Study Identification

Unique Protocol Identification Number
NCT00284466
Brief Title
Comparing Angiography: Multislice CT Versus Invasive Heart Catheterization (CACTI)
Official Title
Comparing Angiography: Multislice CT vs. Invasive Heart Catheterization (CACTI)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
August 2006 (Actual)
Study Completion Date
August 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Wisconsin, Madison

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to compare the pictures of heart arteries obtained by MSCT scanner to the pictures obtained during heart catheterization. Our specific question is whether the MSCT scanner is accurate enough to replace heart catheterization in some situations for the evaluation of coronary heart disease.
Detailed Description
QUESTION: Compare the accuracy of multi-slice CT angiography (CTA) with invasive catheterization (Cath) in detecting and grading coronary lesions. EXPERIMENTAL DESIGN: A prospective cohort analysis comparing the quantification of coronary atherosclerosis by Computed Tomographic angiography to that of invasive Catheterization. Subjects will be patients who are scheduled for non-urgent cardiac cath based on a clinical need to evaluate the coronary anatomy. Cath may be scheduled after a positive stress test or on the basis of concerning symptoms. If a patient consents to participation they will be scheduled for CTA no less than 3 and no more than 30 days prior to Cath. Comparison of lesions detected by the two imaging modalities in the proximal, mid and distal coronary arteries will be made. Grades of disease used will be the following 1). less than 50% 2). 50-75% 3). greater than 75% 4) Uninterpretable. Sensitivity and specificity will be calculated for CTA; in addition PPV and NPV will also be calculated. The 2 readers of the CTA will be blinded to the invasive angiography results. The 2 readers of the invasive angiography, who are blinded to the CTA results will be the standard of comparison. Analysis of data will be performed on a segmental, vessel, and patient basis. POTENTIAL RISK: Risks associated with contrast exposure include the risk of allergic reaction and renal injury. There is a small risk of excessive bradycardia and hypotension with administration of metoprolol and nitroglycerine. CTA is associated with radiation exposure similar to the lower range of diagnostic catheterization. POTENTIAL BENEFITS: No direct benefits are expected for the subjects of this study as the information will not be used to alter clinical decisions. Benefits to future patients may include the development of an non-invasive alternative to cardiac catheterization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Arteriosclerosis
Keywords
coronary artery disease, cardiac catheterization, CT coronary angiography, coronary angiography

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
MS-CT Coronary Angiography
Intervention Description
MS-CT Coronary Angiography done
Primary Outcome Measure Information:
Title
The primary endpoint of the study is the ability of CTA to detect coronary disease of greater than 50% diameter stenosis (sensitivity, specificity, positive and negative predictive value) analyzed on a subject basis.
Time Frame
assess at time of CTA
Secondary Outcome Measure Information:
Title
Assess CTA performance on both a vessel and coronary segment basis
Time Frame
assessed at time of CTA
Title
Estimate the impact of coronary calcium score on ability to assess for coronary disease
Time Frame
assessed at time of CTA
Title
Evaluate impact of scan quality of CTA performance measures
Time Frame
assessed at time of CTA

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects >18 years old with stable clinical symptoms who are scheduled for outpatient cardiac catheterization. Able to provide written informed consent in accordance with the IRB. Exclusion Criteria: Symptoms of unstable angina/acute coronary syndrome Known allergy or adverse reaction to CT radiocontrast and/or iodine. Known absolute contraindication to Metoprolol. Significant kidney disease including creatinine > 1.5 mg/dL or GFR < 60 ml/min. Inability to breath-hold for up to 30 seconds. Women who are Pregnant or Nursing Atrial Fibrillation or any other arrhythmia that makes attaining a regular slow rhythm unlikely. History of previous stent placement or coronary bypass surgery.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jon G Keevil, MD
Organizational Affiliation
University of Wisconsin, Madison
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Wisconsin
City
Madison
State/Province
Wisconsin
ZIP/Postal Code
53792
Country
United States

12. IPD Sharing Statement

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Comparing Angiography: Multislice CT Versus Invasive Heart Catheterization (CACTI)

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