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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05817695
Other study ID # MICRA-SYNK-001
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 1, 2022
Est. completion date May 31, 2023

Study information

Verified date December 2022
Source First People's Hospital of Hangzhou
Contact Yi zhou XU
Phone +8657156005600
Email mage0311@163.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Comparison of cardiac synchronization and tricuspid regurgitation with or without leadless pacemaker pacing in different site


Description:

Right ventricular pacing might lead to pacing-induced cardiomyopathy by dyssynchrony and tricuspid regurgitation. Pacing at various sites had different effects on synchrony and tricuspid regurgitation. This study is to observe the effect of leadless pacemaker implantation in different regions on ventricular synchronization and tricuspid regurgitation. Ultrasound and ECG parameter indices are applied.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date May 31, 2023
Est. primary completion date May 1, 2023
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: patients consent to LP implantation surgery Exclusion Criteria: 1. Patients with inferior vena cava thrombus, a cancer thrombus, an abnormal inferior vena cava; 2. Patients with femoral vein stenosis and tortuosity failed to accommodate the pacemaker delivery system; 3. Patients with myocardial infarction; 4. Patients who have been implanted with devices that affect the pacemaker delivery system, such as vena cava filters or tricuspid valve mechanical valves; 5. cannot understand or are unwilling to give informed consent.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Leadless pacemaker
To observe the effect of pacemaker implantation at different sites on cardiac synchronization and tricuspid regurgitation

Locations

Country Name City State
China Yi zhou XU Hangzhou Zhejiang

Sponsors (2)

Lead Sponsor Collaborator
First People's Hospital of Hangzhou Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The evaluation of cardiac electrical synchrony the QRS duration after pacing 1 month
Primary The evaluation of cardiac mechanical synchrony ?Synchronization analysis between left and right ventricles: interventricular mechanical delay (IVMD) in millisecond.
?Left ventricle synchrony analysis: septal-to-posterior wall motion delay (SPWMD) in millisecond,left pre-ejection interval(LPEI) in millisecond.
1 month
Secondary Age may affect synchronization Age in years 1 month
Secondary BMI may affect synchronization BMI in kg/m^2 1 month
Secondary Blood pressure may affect synchronization Systolic and diastolic blood pressure in mmHg 1 month
Secondary The pacemaker sensing may affect synchronization pacemaker sensing in millivolt 1 month
Secondary The pacemaker lead impedance may affect synchronization lead impedance in ohm 1 month
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