Measurement of Left and Right Atria From CT Scans of Cardiac Rhythm Disorder Cases
This study is currently recruiting participants.
Verified April 2012 by Kardium Inc.
Sponsor:
Kardium Inc.
Collaborator:
St. Paul's Hospital, Canada
Information provided by (Responsible Party):
Kardium Inc.
ClinicalTrials.gov Identifier:
NCT01165593
First received: July 16, 2010
Last updated: April 4, 2012
Last verified: April 2012
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Purpose
The purpose of this study is to gather information about the size and shape of patients' hearts in order to design a device. Correct device design depends on getting good information about the shape and size of the different parts of the heart. Measurements from computed tomography images of hearts will be studied. By looking at measurements from a wide range of patients, an understanding of the differences in the size and shape of the heart chambers will be gained.
| Condition | Intervention |
|---|---|
|
Atrial Fibrillation |
Other: There is no intervention that is a part of this study. |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Retrospective |
| Official Title: | Measurement of Left and Right Atria From CT Scans of Cardiac Rhythm Disorder Cases |
Resource links provided by NLM:
Further study details as provided by Kardium Inc.:
| Estimated Enrollment: | 100 |
| Study Start Date: | August 2010 |
| Estimated Study Completion Date: | August 2012 |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Patients with atrial fibrillation
Patients with atrial fibrillation who have received a cardiac CT scan as part of normal care prior to catheter-based treatment of atrial fibrillation.
|
Other: There is no intervention that is a part of this study.
There is no intervention that is a part of this study. Imaging data is gathered as part of normal care.
|
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Patients with atrial fibrillation who are deemed suitable for treatment of atrial fibrillation by catheter-based ablation.
Criteria
Inclusion Criteria:
- Patients deemed suitable for treatment of atrial fibrillation by catheter-based ablation who have received cardiac CT imaging as part of normal care.
Exclusion Criteria:
- Patients who have not received cardiac CT imaging as part or normal care.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01165593
Contacts
| Contact: Carol Honeyman, RN | (604) 682-2344 ext 62464 | |
| Contact: Neil Bulman-Fleming, MEng | 604-248-8891 ext 284 |
Locations
| Canada, British Columbia | |
| St. Paul's Hospital | Recruiting |
| Vancouver, British Columbia, Canada, V6Z 1Y6 | |
| Contact: Carol Honeyman, RN (604) 682-2344 ext 62464 choneyman@providencehealth.bc.ca | |
| Contact: Neil Bulman-Fleming, MEng 604-248-8891 ext 284 neil.bulman-fleming@kardium.com | |
| Principal Investigator: John Yeung-Lai-Wah | |
Sponsors and Collaborators
Kardium Inc.
St. Paul's Hospital, Canada
Investigators
| Principal Investigator: | John A. Yeung-Lai-Wah, MD | St' Paul's Hospital Electrophysiology (Providence Health Care) |
More Information
No publications provided
| Responsible Party: | Kardium Inc. |
| ClinicalTrials.gov Identifier: | NCT01165593 History of Changes |
| Other Study ID Numbers: | H10-01337 |
| Study First Received: | July 16, 2010 |
| Last Updated: | April 4, 2012 |
| Health Authority: | Canada: Ethics Review Committee |
Additional relevant MeSH terms:
|
Arrhythmias, Cardiac Atrial Fibrillation Heart Diseases Cardiovascular Diseases Pathologic Processes |
ClinicalTrials.gov processed this record on May 16, 2013