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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04931550
Other study ID # Y2020-675
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 1, 2020
Est. completion date December 2026

Study information

Verified date January 2023
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Xiaohong Pan
Phone +8613857116993
Email heartpanxh@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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, different sites can be chosen to pace, such as right atrial appendage, the atrial septum and the right atrial wall in the atrium, His bundle, left bundle branch area, right ventricular apex, outflow tract, and left ventricular pacing via coronary vein in the ventricle. There are few studies comparing the long-term efficacy and safety of different pacing sites in daily practice. This study aims to observe the efficacy and safety of cardiac pacing at different sites in short and long term, and to compare the advantages and disadvantages of pacing at different sites.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date December 2026
Est. primary completion date December 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Pacemaker implantation
Different pacing sites will be chosen according to the patients condition.

Locations

Country Name City State
China 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China Hangzhou Zhejiang

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Composite of Cardiovascular death, myocardial infarction, and stroke events Composite of Cardiovascular death, myocardial infarction, and stroke events in 60 months 60 months
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