Non Invasive Multicenter Italian Study for Coronary Artery Disease

NCT ID: NCT00539604

Last Updated: 2007-10-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 350 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-07-31
• Study Completion Date: 2006-06-30

Brief Summary

To determine if 16-64 slice multidetector CT (MDCT) can replace the invasive procedure in patients scheduled for coronary angiography in order to exclude the presence of CAD

Detailed Description

Because coronary artery disease (CAD) is the most frequent cause of death in industrialized nations and its onset is currently unpredictable, there is a need for new methods of screening apparently healthy individuals to identify those at increased risk.

Several imaging techniques are in use to visualize coronary arteries. These include both invasive procedure as x-ray coronary angiography and those non invasive like computed tomography (CT) and magnetic resonance imaging (MRI). Among these imaging modalities, selective cardiac catheterization and x-ray angiography is the current gold standard for visualization of coronaries and detection of their stenoses, providing for optimal spatial resolution, a general "road map" of the coronary tree for interventions. The replacement of even a fraction of these procedures with non-invasive modalities would constitute an important advance in the care of patients with suspected coronary artery disease Preliminary results reported in literature addressing the study of coronary arteries by multidetector-CT (MDCT) appear to be interesting. Several studies have been performed firstly using Electron beam CT (EBCT).EBCT provides high temporal resolution and enables quantitative assessment of the coronary artery calcium, but because of limited spatial resolution as a result of limited z axis resolution, it does not permit direct visualisation in multi-reformation of the whole coronary artery system.

With the introduction of 4-row MDCT there have now been several studies aimed to compare the MDCT with a standard invasive angiography. Data published for over 200 subjects from 4 studies demonstrated that patient compliance at breath-hold, heart rate and rhythm are crucial limitation to this procedure. In the Nieman and Achembach papers not all the coronary segments were assessable because of the limited temporal resolution of 4-slice MDCT. With this machine it is mandatory to select patients carefully, considering only those with baseline hearth rate < 65 bpm (also obtained by pre-treatment with β-blockers in order to slow hearth rate).

Conditions

Coronary Heart Disease

Keywords

Comparison study between MDCT and coronary angiography

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Interventions

MDCT and Coronary Angiography

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Patients (men or women of any ethnic group) scheduled for a coronary angiography evaluation for a diagnostic work up.

2. Patients will be expected to undergo coronary angiography within 2 weeks after the MDCT study procedure. The coronary angiography must meet the minimum standard laid down in the protocol (see section 8.3.3).

3. Patients must have HDL and total cholesterol performed within the last year.

4. Patients must be willing and able to continue study participation following the reference test to ensure completion of all procedures and observations required by the study.

5. Fully informed and signed consent must be obtained from each patient.

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Exclusion Criteria

1. Patients under 18 years of age.

2. Patients who have received any investigational drug within the 30 days prior to entering this study.

3. Pregnant or lactating women.

4. Patients who have any contraindication to MDCT examination with iodinate contrast media.

5. Patients with heart rate >70 bpm despite of β-blocker treatment (see section 8.2.4.1).

6. Patients with no sinus rhythm.

7. Patients with NYHA III or IV class.

8. Patients who have previously undergone CABG or stenting.

9. Patients with a creatinine value > 2 mg/dl.

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• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Società Italiana di Radiologia Medica

OTHER

Sponsor Role: lead

Principal Investigators

Alessandro Del Maschio, Med. Doctor

Role: PRINCIPAL_INVESTIGATOR

Lorenzo Bonomo, Med. Doctor

Role: PRINCIPAL_INVESTIGATOR

Locations

Policlinico di Bari Istituto di Radiologia

Bari, Ba, Italy

Policlinico S. Orsola Malpighi Istituto di Radiologia III

Bologna, Bo, Italy

Azienda Istituti Ospitalieri U.O. Radiologia

Cremona, CR, Italy

Istituti clinici Humanitas

Rozzano, Milano, Italy

Ospedale San Raffaele Istituto di Radiologia

Milan, MI, Italy

Centro Cardiologico Monzino Servizio di Radiologia

Milan, MI, Italy

Policlinico di Modena Istituto di Radiologia

Modena, Mo, Italy

Ospedale G. Pasquinucci Unità Operativa di Radiologia

Massa, Ms, Italy

Policlinico P. Giaccone Dip. Scienze Radiologiche

Palermo, Pa, Italy

A.O. Riuniti Unità Operativa di Radiologia

Reggio Calabria, R.C., Italy

Policlinico Le Scotte DAI dell' Immagine

Siena, SI, Italy

A.O. S. Maria Dipartimento di Diagnostica per Immagini

Terni, TN, Italy

Ospedale S. Chiara Dipartimento di Radiologia

Trento, TN, Italy

Ospedale Molinette Istituto di Radiologia

Torino, To, Italy

Ospedale S. Maria di Ca' Foncello U.C. Radiologia

Treviso, TV, Italy

A.O.R.N. Cardarelli Radiologia Generale I Sez.

Napoli, , Italy

Policlinico Tor Vergata Istituto di Radiologia

Roma, , Italy

Policlinico Umberto I Radiologia D.E.A.

Roma, , Italy

Policlinico Umberto I Università degli Studi "La Sapienza" Dip. Scienze Radiologiche

Roma, , Italy

Policlinico Gemelli Istituto di Radiologia

Roma, , Italy

Countries

Italy

Other Identifiers

NIMIS-CAD

Identifier Type: -

Identifier Source: org_study_id