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Individuals receiving conduction system pacing for Bradyarrhythmias
N/A
Recruiting
Led By Roderick Tung, MD
Research Sponsored by University of Chicago
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Meets American College of Cardiology (ACC)/American Heart Association (AHA)/Heart Rhythm Society (HRS) guidelines for bradycardia, or * Meets ACC/AHA/HRS guidelines for cardiac resynchronization therapy (CRT).
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through 12 months
Awards & highlights
Summary
The purpose of this registry study is to collect information about routine clinical practices with device implantation to treat bradycardia and cardiac systolic dysfunction (heart rhythm disorders) across global centers of excellence in cardiac pacing. In particular, this study will examine the use of conduction system pacing (CSP) in clinical practice. Information collected in the registry will help researchers better characterize strengths and limitations of current technology and treatments.
Eligible Conditions
- Bradyarrhythmias
- Heart Failure
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through 12 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Any-cause mortalities
Changes in chamber dimension
Changes in left ventricular ejection fraction
+10 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Individuals receiving conduction system pacingExperimental Treatment1 Intervention
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Who is running the clinical trial?
Biotronik SE & Co. KGIndustry Sponsor
111 Previous Clinical Trials
46,871 Total Patients Enrolled
University of ChicagoLead Sponsor
1,036 Previous Clinical Trials
757,729 Total Patients Enrolled
Roderick Tung, MDPrincipal InvestigatorUniversity of Chicago
5 Previous Clinical Trials
473 Total Patients Enrolled
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