NCT01142973

Brief Summary

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

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
5,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Sep 2005

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2005

Completed
4.8 years until next milestone

First Submitted

Initial submission to the registry

June 11, 2010

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 14, 2010

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2010

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2010

Completed
Last Updated

September 13, 2010

Status Verified

September 1, 2010

Enrollment Period

4.9 years

First QC Date

June 11, 2010

Last Update Submit

September 10, 2010

Conditions

Outcome Measures

Primary Outcomes (1)

  • Major cardiovascular events

    Cardiovascular death, non-fatal MI, or any stroke

    1 years after the MDCT-scan

Secondary Outcomes (1)

  • all causes of hospitalization

    1 years after the MDCT-scan

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

present typical/atypical chest pain

You may qualify if:

  • Patients with known or suspected coronary artery disease

You may not qualify if:

  • Irregular heart beat
  • Known allergy towards the contrast agent
  • Renal dysfunction
  • Impossible breath-hold
  • Acute coronary syndrome patient

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ilsan Paik hospital

Goyang, South Korea

RECRUITING

Related Publications (1)

  • Kim JB, Rogers IS, Kwon SU. Presence of plaques predicts worse outcomes in multi-detector computed tomography in patients with stable chest pain syndrome. Int J Cardiol. 2014 May 15;173(3):570-2. doi: 10.1016/j.ijcard.2014.03.118. Epub 2014 Mar 21. No abstract available.

MeSH Terms

Conditions

AtherosclerosisCardiovascular DiseasesCoronary Artery Disease

Condition Hierarchy (Ancestors)

ArteriosclerosisArterial Occlusive DiseasesVascular DiseasesCoronary DiseaseMyocardial IschemiaHeart Diseases

Study Officials

  • Sung Uk Kwon, M.D.

    Inje univ. ilsan paik hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Sung Uk Kwon, M.D.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

June 11, 2010

First Posted

June 14, 2010

Study Start

September 1, 2005

Primary Completion

August 1, 2010

Study Completion

December 1, 2010

Last Updated

September 13, 2010

Record last verified: 2010-09

Locations