NCT00566059

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started May 2006

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

May 1, 2006

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2007

Completed
7 months until next milestone

First Submitted

Initial submission to the registry

November 30, 2007

Completed
3 days until next milestone

First Posted

Study publicly available on registry

December 3, 2007

Completed
Last Updated

December 3, 2007

Status Verified

November 1, 2007

First QC Date

November 30, 2007

Last Update Submit

November 30, 2007

Conditions

Coronary Artery DiseaseCoronary Artery Stenosis

Keywords

therapeutic advice

Eligibility Criteria

Age50 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients over 50 years of age, scheduled for elective coronary angiography

You may qualify if:

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

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Medical Center Groningen

Groningen, Netherlands

Location

MeSH Terms

Conditions

Coronary Artery DiseaseCoronary Stenosis

Condition Hierarchy (Ancestors)

Coronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesArteriosclerosisArterial Occlusive DiseasesVascular Diseases

Study Officials

  • Felix Zijlstra, MD PhD

    University Medical Center Groningen

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER

Study Record Dates

First Submitted

November 30, 2007

First Posted

December 3, 2007

Study Start

May 1, 2006

Study Completion

May 1, 2007

Last Updated

December 3, 2007

Record last verified: 2007-11

Locations

NL(1)