NCT01165593

Brief Summary

The purpose of this study is to gather information about the size and shape of patients' hearts in order to design a device.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
96

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 2010

Typical duration 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

First Submitted

Initial submission to the registry

July 16, 2010

Completed
4 days until next milestone

First Posted

Study publicly available on registry

July 20, 2010

Completed
3 months until next milestone

Study Start

First participant enrolled

November 1, 2010

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2013

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2013

Completed
Last Updated

April 16, 2015

Status Verified

April 1, 2015

Enrollment Period

2.9 years

First QC Date

July 16, 2010

Last Update Submit

April 15, 2015

Conditions

Atrial Fibrillation

Outcome Measures

Primary Outcomes (1)

  • LA size measurements

    3 months

Study Arms (1)

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.

Interventions

There is no intervention that is a part of this study.OTHER

There is no intervention that is a part of this study. Imaging data is gathered as part of normal care.

Patients with atrial fibrillation

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with atrial fibrillation who are deemed suitable for treatment of atrial fibrillation by catheter-based ablation.

You may qualify if:

  • Patients deemed suitable for treatment of atrial fibrillation by catheter-based ablation who have received cardiac CT imaging as part of normal care.

You may not qualify if:

  • Patients who have not received cardiac CT imaging as part or normal care.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

St. Paul's Hospital

Vancouver, British Columbia, V6Z 1Y6, Canada

Location

MeSH Terms

Conditions

Atrial Fibrillation

Condition Hierarchy (Ancestors)

Arrhythmias, CardiacHeart DiseasesCardiovascular DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • John A. Yeung-Lai-Wah, MD

    St' Paul's Hospital Electrophysiology (Providence Health Care)

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 16, 2010

First Posted

July 20, 2010

Study Start

November 1, 2010

Primary Completion

October 1, 2013

Study Completion

October 1, 2013

Last Updated

April 16, 2015

Record last verified: 2015-04

Locations

CA(1)