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

This study has been completed.
Sponsor:
Information provided by:
University Medical Centre Groningen
ClinicalTrials.gov Identifier:
NCT00566059
First received: November 30, 2007
Last updated: NA
Last verified: November 2007
History: No changes posted
  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

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by University Medical Centre Groningen:

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

Ages Eligible for Study:   50 Years and older
Genders Eligible for Study:   Both
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
Please refer to this study by its ClinicalTrials.gov identifier: NCT00566059

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

No publications provided

Responsible Party: F. Zijlstra, University Medical Center Groningen
ClinicalTrials.gov Identifier: NCT00566059     History of Changes
Other Study ID Numbers: CARDUCCI
Study First Received: November 30, 2007
Last Updated: November 30, 2007
Health Authority: Netherlands: Medical Ethics Review Committee (METC)

Keywords provided by University Medical Centre 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

ClinicalTrials.gov processed this record on May 16, 2013