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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00566059
Other study ID # CARDUCCI
Secondary ID
Status Completed
Phase N/A
First received November 30, 2007
Last updated November 30, 2007
Start date May 2006
Est. completion date May 2007

Study information

Verified date November 2007
Source University Medical Center Groningen
Contact n/a
Is FDA regulated No
Health authority Netherlands: Medical Ethics Review Committee (METC)
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility 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.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
Netherlands University Medical Center Groningen Groningen

Sponsors (1)

Lead Sponsor Collaborator
University Medical Center Groningen

Country where clinical trial is conducted

Netherlands, 

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