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

This study has been completed.
Sponsor:
Information provided by:
Charite University, Berlin, Germany
ClinicalTrials.gov Identifier:
NCT00968279
First received: August 27, 2009
Last updated: May 2, 2013
Last verified: April 2013
  Purpose

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.


Condition
Atrial Fibrillation

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Coronary CT Angiography Using 320-Row Volume CT in Patients With Atrial Fibrillation

Resource links provided by NLM:


Further study details as provided by Charite University, Berlin, Germany:

Enrollment: 54
Study Start Date: August 2009
Study Completion Date: September 2012
Primary Completion Date: September 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
Atrial Fibrillation

  Eligibility

Ages Eligible for Study:   50 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients with atrial fibrillation scheduled to undergo coronary angiography due to suspected coronary artery disease.

Criteria

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
  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: NCT00968279

Locations
Germany
Charité
Berlin, Germany, 10117
Sponsors and Collaborators
Charite University, Berlin, Germany
Investigators
Principal Investigator: Marc Dewey, MD, PhD Charité
  More Information

Publications:
Responsible Party: Marc Dewey, Charité
ClinicalTrials.gov Identifier: NCT00968279     History of Changes
Other Study ID Numbers: EA1/134/08
Study First Received: August 27, 2009
Last Updated: May 2, 2013
Health Authority: Germany: Federal Department for Radiation Protection

Keywords provided by Charite University, Berlin, Germany:
Patients with atrial fibrillation

Additional relevant MeSH terms:
Atrial Fibrillation
Arrhythmias, Cardiac
Heart Diseases
Cardiovascular Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on September 30, 2014