Zero-fluoroscopic Navigation Versus Conventional Fluoroscopic Navigation for Single-chamber Pacemaker Implantation

NCT03118440 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2017-04-18

No results posted yet for this study

Summary

This study is intended to compare the feasibility, safety and efficacy of Ensite-NavX zero-fluoroscopic navigation system to conventional fluoroscopic X-ray approach as to performing single-chamber pacemaker implantation.

Conditions

  • Sick Sinus Syndrome
  • Complete Atrioventricular Block
  • High Degree Second Degree Atrioventricular Block
  • Bradycardia

Interventions

PROCEDURE

zero-fluoroscopy 3D navigation

Pacemaker implantation will be performed without fluoroscopy using 3D navigation systems.

PROCEDURE

conventional x-ray navigation

Pacemaker implantation will be performed with fluoroscopy using conventional X-ray navigation.

Sponsors & Collaborators

  • Fu Wai Hospital, Beijing, China

    collaborator OTHER
  • Xinyang Central Hospital

    collaborator OTHER
  • First Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • Wuhan Asia Heart Hospital

    collaborator OTHER
  • Shenzhen Sun Yat-sen Cardiovascular Hospital

    collaborator OTHER
  • Ningbo No. 1 Hospital

    collaborator OTHER
  • Tongji Hospital

    lead OTHER

Principal Investigators

  • Yan Wang, PhD · Tongji Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2018-12-31
Completion
2020-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03118440 on ClinicalTrials.gov