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Device
VDD ICD (experimental group) for Cardiovascular Disease (Dx-AF Trial)
N/A
Waitlist Available
Led By Eugene Crystal, MD, FRCP(C)
Research Sponsored by Unity Health Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up during the entire time of follow up - 3 years
Awards & highlights
Dx-AF Trial Summary
This trial will compare two different ICD systems on their ability to detect silent AFib in patients without a history of AFib.
Eligible Conditions
- Cardiovascular Disease
- Arrhythmia
- Atrial Fibrillation or Atrial Flutter
- Implantable Cardioverter Defibrillators
Dx-AF Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ during the entire time of follow up - 3 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~during the entire time of follow up - 3 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Atrial Fibrillation or atrial flutter lasting at least 6 minutes
Secondary outcome measures
Cardiac tamponade
Need for any ICD lead repositioning or replacement
New pericardial effusion
+2 moreDx-AF Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: VDD ICDExperimental Treatment1 Intervention
VDD ICD - A single-lead ICD system with the ability to sense atrial rhythm from the floating electrode (a VDD-ICD known as the DX) - Experimental group
Group II: VVI ICDActive Control1 Intervention
VVI ICD - Single chamber ICD system - Control group
Find a Location
Who is running the clinical trial?
Unity Health TorontoLead Sponsor
536 Previous Clinical Trials
447,341 Total Patients Enrolled
Applied Health Research CentreOTHER
22 Previous Clinical Trials
70,848 Total Patients Enrolled
Biotronik Canada IncIndustry Sponsor
4 Previous Clinical Trials
1,684 Total Patients Enrolled
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