Zero Fluoroscopic Ablation Versus Conventional Fluoroscopic Ablation for Right Atrial Arrhythmias

NCT03151278 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 212

Last updated 2023-11-24

No results posted yet for this study

Summary

This study is intended to compare the feasibility, safety and efficacy of a zero-fluoroscopic approach with conventional fluoroscopic approach as performing catheter ablation of right atrial arrhythmias.

Conditions

  • Atrial Arrhythmia
  • Atrial Premature Complexes
  • Atrial Tachycardia

Interventions

PROCEDURE

Zero-fluoroscopy ablation

Catheter ablation will be performed under the guidance of one kind of three-dimensional navigation system and without fluoroscopic guidance.

PROCEDURE

Conventional fluoroscopy ablation

Catheter ablation will be performed using fluoroscopy plus one kind of three-dimensional navigation system.

Sponsors & Collaborators

  • Fu Wai Hospital, Beijing, China

    collaborator OTHER
  • Xinyang Central Hospital

    collaborator OTHER
  • Ningbo No. 1 Hospital

    collaborator OTHER
  • Shanghai Tongji Hospital, Tongji University School of Medicine

    collaborator OTHER
  • First Affiliated Hospital of Guangxi Medical University

    collaborator OTHER
  • Shenzhen Sun Yat-sen Cardiovascular Hospital

    collaborator OTHER
  • Guangdong Provincial People's Hospital

    collaborator OTHER
  • Zhongshan Hospital Xiamen University

    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
2011-01-31
Primary Completion
2017-12-31
Completion
2018-12-31

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 NCT03151278 on ClinicalTrials.gov