Coronary CT Angiography Using 320-Row Volume CT in Patients With Atrial Fibrillation

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00968279

Enrollment

Registered

2009-08-28

Start date

2009-08-31

Completion date

2012-09-30

Last updated

2013-05-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

Keywords

Patients with atrial fibrillation

Brief summary

The primary objective of this study is to analyze the diagnostic accuracy of coronary CT angiography using 320 simultaneous detector results in patients with atrial fibrillation.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

50 Years to No maximum

Healthy volunteers

Inclusion criteria

* Suspected coronary artery disease based on clinical findings or findings on other noninvasive imaging tests and planned coronary angiography within the next 14 days. * Able to understand and willing to sign the Informed CF.

Exclusion criteria

* Creatinine of above 2.0 mg/dl * Age below 50 years * Women of child bearing potential (no hysterectomy, no menopause, or menopause since less than 12 months) must demonstrate a negative pregnancy test performed within 24 hours before CT. * Inability to hold the breath for 10 seconds

Countries

Germany

Outcome results