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Computed Tomographic Angiography or Conventional Coronary Angiography in Clinical Decision Making (CARDUCCI)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00566059
First Posted: December 3, 2007
Last Update Posted: December 3, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
University Medical Center Groningen
  Purpose
Patients planned for elective conventional coronary angiography will undergo CT coronary angiography (Dual Source CT) in order to assess the correlation of stenosis detection and therapeutic advice between conventional and CT coronary angiography. We hypothesize that their is a good correlation between conventional and CT coronary angiography for stenosis detection and therapeutic advice.

Condition
Coronary Artery Disease Coronary Artery Stenosis

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Comparison Between Invasive Coronary Angiography and Dual-Source Computed Tomography

Further study details as provided by University Medical Center Groningen:

Enrollment: 60
Study Start Date: May 2006
Study Completion Date: May 2007
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   50 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients over 50 years of age, scheduled for elective coronary angiography
Criteria

Inclusion Criteria:

  • Over 50 years of age
  • Scheduled for elective coronary angiography

Exclusion Criteria:

  • Patients with known iodine allergy
  • Severe renal insufficiency (creatinine levels > 120 micromol/L)
  • Hyperthyroidism
  • Cardiac arrhythmias
  • Unstable clinical condition
  • Inability to follow breath-hold commands
  • Previous PCI or CABG were excluded.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00566059


Locations
Netherlands
University Medical Center Groningen
Groningen, Netherlands
Sponsors and Collaborators
University Medical Center Groningen
Investigators
Study Director: Felix Zijlstra, MD PhD University Medical Center Groningen
  More Information

Responsible Party: F. Zijlstra, University Medical Center Groningen
ClinicalTrials.gov Identifier: NCT00566059     History of Changes
Other Study ID Numbers: CARDUCCI
First Submitted: November 30, 2007
First Posted: December 3, 2007
Last Update Posted: December 3, 2007
Last Verified: November 2007

Keywords provided by University Medical Center Groningen:
therapeutic advice

Additional relevant MeSH terms:
Coronary Artery Disease
Myocardial Ischemia
Coronary Disease
Coronary Stenosis
Heart Diseases
Cardiovascular Diseases
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases