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Clinical Trials/NCT04919447
NCT04919447
Recruiting
Not Applicable

Study of the Efficacy and Safety of Cardiac Pacing of Different Sites

Second Affiliated Hospital, School of Medicine, Zhejiang University1 site in 1 country540 target enrollmentJune 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Bradyarrhythmias
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Enrollment
540
Locations
1
Primary Endpoint
Composite of Cardiovascular death, myocardial infarction, and stroke events
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

At present, cardiac pacing has been widely used in the treatment of bradyarrhythmias and heart failure, which can effectively improve the survival rate of patients. With the rapid development of technology, you can choose to pace the heart in different parts. The atrium can choose the right atrial appendage, the atrial septum and the right ventricular side wall. The right ventricle can choose to be paced in the His bundle, right ventricular apex and ventricular septal outflow tract. The right ventricle can choose the pacing positions including left bundle branch pacing and left ventricular pacing via coronary vein. There are few studies comparing the long-term efficacy and safety of different pacing programs in daily practice. This study is to observe the short-term and long-term effects and safety of different parts of cardiac pacing, and compare the advantages and disadvantages of different parts of cardiac pacing.

Registry
clinicaltrials.gov
Start Date
June 1, 2021
End Date
August 2025
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients who received pacemaker implantation in the Second Hospital of Zhejiang Medical University by Pan Xiaohong and other surgeons.
  • Patients who have the ability to understand the test and can cooperate with investigators.

Exclusion Criteria

  • Patients who unable to understand or unwilling to fill in informed consent forms or follow visitors

Outcomes

Primary Outcomes

Composite of Cardiovascular death, myocardial infarction, and stroke events

Time Frame: 60 months

Study Sites (1)

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