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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00468325
Other study ID # 2007-016
Secondary ID
Status Completed
Phase N/A
First received April 30, 2007
Last updated November 13, 2009
Start date May 2007
Est. completion date May 2009

Study information

Verified date November 2009
Source William Beaumont Hospitals
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

This is a prospective, randomized multicenter trial comparing MSCT to standard of care (SOC) diagnostic treatment in the triage of Emergency Department (ED) low to intermediate risk chest pain patients. Our hypotheses are that compared to SOC treatment, MSCT is equally safe and diagnostically effective, as well as more time and cost efficient.


Description:

Computed tomography (CT) or "cat scan" is an x-ray test routinely used for diagnostic purposes. Heart ("Cardiac") CT, using the newest scanners, is an improved way of looking at the coronary arteries, which supply blood to the heart muscle. If these arteries are clogged this may cause chest pain or even a heart attack. The images of the coronary arteries obtained by CT scanners (during a 5-10 minute procedure) have been shown by many studies to be accurate, when compared to the conventional invasive cardiac catheterization procedure. In addition, at least five prior studies done at different hospitals suggest that cardiac CT scans are effective for diagnosing chest pain like yours in patients coming to the emergency room. What is new about this study is that it is being done in multiple hospitals at the same time. This is part of the process that all medical advances must go through to become a part of routine care of patients in hospitals throughout the country.

A standard chest pain workup typically done in the emergency department consists of a physical examination, electrocardiograms (EKGs), and several blood tests. Blood tests typically completed include cardiac enzymes (Troponin, CK & CK-MB), a kidney function test, a pregnancy test if applicable, and possibly a lipid panel, depending on physician preference. For each test, a 3mL vial will be filled with a specimen of blood and processed in the laboratory for result. Also a two-part "rest-stress" nuclear scan is typically performed, which compares blood flow into the heart tissue at rest to blood flow into the heart tissue during exercise or dilation with medications. Based on prior studies, the researchers doing the present study believe that CT scanning of the coronary arteries can provide information that is just as safe and accurate as the rest-stress nuclear scan, and can do so more rapidly at a lower cost.


Recruitment information / eligibility

Status Completed
Enrollment 750
Est. completion date May 2009
Est. primary completion date November 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 25 Years and older
Eligibility Inclusion Criteria:

- Chest pain or anginal equivalent symptoms suggestive of acute coronary ischemia within the past 12 hours.

- TIMI risk score less than or equal to 4.

- Ability to provide informed consent.

- Age greater than or equal to 25 years.

Exclusion Criteria:

- Attending physician makes clinical decision for immediate invasive evaluation.

- Electrographic evidence of ischemia, including acute Non ST-Elevation Myocardial Infarction (NSTEMI) or ST-Elevation Myocardial Infarction (STEMI), with ST segment elevation or depression equal to or greater than 1mm in two or more contiguous leads, and/or T wave inversion greater than or equal to 2 mm.

- Positive cardiac biomarkers (troponin, CK, and/or CK-MB) compatible with AMI on initial laboratory testing, based on site standard laboratory values.

- Presence of pre-existing CAD, including prior MI, prior angiographic evidence of significant CAD, defined as greater than or equal to 25% stenosis, or history of coronary artery bypass graft (CABG) surgery.

- Renal insufficiency (creatinine greater than 1.5 mg/dL) or renal failure requiring dialysis.

- Atrial fibrillation or other markedly irregular rhythm.

- Psychological unsuitability or extreme claustrophobia.

- Pregnancy or unknown pregnancy status.

- Clinical instability including cardiogenic shock, hypotension (systolic blood pressure <90 mmHg), refractory hypertension (systolic blood pressure >180 mmHg on therapy), sustained ventricular or atrial arrhythmia requiring intravenous medications.

- Known allergy to iodine or iodinated contrast.

- Inability to tolerate beta-blocker medication, including patients with asthma or chronic obstructive pulmonary disease (COPD) requiring maintenance, i.e. use of inhaled bronchodilators or steroids, or patients with complete heart block or second-degree atrioventricular block.

- Iodinated contrast administration or x-ray scan within the past 48 hours.

- Use of any erectile dysfunction medications such as Viagra or Cialis in the last 24 hours.

- Body Mass Index (BMI) greater than or equal to 39 kg/m2. . Use of biguanides within the past 48 hours

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Procedure:
Multi-slice computed tomography
Patient receives a CT scan (multi-slice computed tomography) of the heart.
Rest-stress Nuclear Myocardial Perfusion Imaging
Patient receives the standard of care for emergency room admitting diagnosis of low to intermediate chest pain. A rest-stress nuclear myocardial perfusion imaging test is performed per the standard of care at each institution.
Multi-slice Computed Tomography
Patients admitted to the emergency department with low to intermediate chest pain receive a multi-slice computed tomographic test of the heart.

Locations

Country Name City State
United States Faqua Heart Center/Piedmont Hospital Atlanta Georgia
United States Massachusetts General Hospital Boston Massachusetts
United States Medical University of South Carolina Charleston South Carolina
United States Northwestern Memorial Hospital Chicago Illinois
United States Metrohealth Medical Center Cleveland Ohio
United States Texas Heart Institute Houston Texas
United States Cedars-Sinai Medical Center Los Angeles California
United States Minneapolis Heart Institute Minneapolis Minnesota
United States Mt Sinai Hospitl New York New York
United States MultiCare Health System-Good Samaritan Hospital Puyallup Washington
United States William Beaumont Hospital Royal Oak Michigan
United States St. Paul Heart Clinic St. Paul Minnesota
United States William Beaumont-Troy Troy Michigan
United States Washington Hospital Center Washington Dc District of Columbia
United States Wisconsin Heart & Vascular Center Wauwatosa Wisconsin
United States Cleveland Clinic Florida Weston Florida

Sponsors (1)

Lead Sponsor Collaborator
William Beaumont Hospitals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Diagnostic efficiency from the time to diagnosis and cost of diagosis for the CCTA and the Standard of Care Time to diagnosis Yes
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