The Clinical Course of Coronary Artery Disease in Coronary Multidetector Computed Tomographic Angiogram (PREDICT)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified September 2010 by Inje University.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
Inje University
ClinicalTrials.gov Identifier:
NCT01142973
First received: June 11, 2010
Last updated: September 10, 2010
Last verified: September 2010
  Purpose

Study Type: Observational Study Design: Observational Model: Defined Population Observational Model: Natural History Time Perspective: Longitudinal Time Perspective: Prospective


Condition
Atherosclerosis
Cardiovascular Diseases
Coronary Artery Disease

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Prognostic Role of Coronary Artery plaquEs in Patients With Suspected Coronary Artery Disease Using Multislice of Computed Tomography (PREDICT)

Resource links provided by NLM:


Further study details as provided by Inje University:

Primary Outcome Measures:
  • Major cardiovascular events [ Time Frame: 1 years after the MDCT-scan ] [ Designated as safety issue: No ]
    Cardiovascular death, non-fatal MI, or any stroke


Secondary Outcome Measures:
  • all causes of hospitalization [ Time Frame: 1 years after the MDCT-scan ] [ Designated as safety issue: No ]
    Requiring hospitalization


Estimated Enrollment: 5000
Study Start Date: September 2005
Estimated Study Completion Date: December 2010
Primary Completion Date: August 2010 (Final data collection date for primary outcome measure)
Detailed Description:

The natural history of individual plaques is unknown and needs to be established. Multidetector computed tomography (MDCT) angiography is a useful noninvasive imaging modality for assessing coronary plaque. Using MDCT, the researchers prospectively investigate the relationship between the presence of coronary plaques and cardiovascular events

  Eligibility

Ages Eligible for Study:   18 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

present typical/atypical chest pain

Criteria

Inclusion Criteria:

  • Patients with known or suspected coronary artery disease

Exclusion Criteria:

  • Irregular heart beat
  • Known allergy towards the contrast agent
  • Renal dysfunction
  • Impossible breath-hold
  • Acute coronary syndrome patient
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01142973

Contacts
Contact: Sung Uk Kwon, M.D. 82-31-910-7041 prof.mdksu@gmail.com

Locations
Korea, Republic of
Ilsan Paik hospital Recruiting
Goyang, Korea, Republic of
Contact: Sung Uk Kwon, M.D.    82-31-910-7041    prof.mdksu@gmail.com   
Sponsors and Collaborators
Inje University
Investigators
Principal Investigator: Sung Uk Kwon, M.D. Inje univ. ilsan paik hospital
  More Information

No publications provided by Inje University

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: Assistant professor, Inje university ILSAN paik hospital
ClinicalTrials.gov Identifier: NCT01142973     History of Changes
Other Study ID Numbers: mdksu-mdct-001
Study First Received: June 11, 2010
Last Updated: September 10, 2010
Health Authority: Korea: Institutional Review Board

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

ClinicalTrials.gov processed this record on October 21, 2014