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A Real-world Study of Cardiac Ablation for PSVT Using ST Catheter

NCT04923815 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2022-02-23

No results posted yet for this study

Summary

Paroxysmal supraventricular tachycardia known as PSVT includes atrioventricular reentrant tachycardia (AVRT) and atrioventricular nodal reentrant tachycardia (AVNRT).

This study is multicenter, retrospective, cohort study. This study will collect real world data of AVNRT and AVRT cohorts retrospectively to evaluate the effectiveness and safety in real world clinical practice. 300 subjects with PSVT will be consecutively enrolled backwards since 02 Nov 2017, and at least 100 subjects for each cohort.

Cohort one: AVNRT Cohort two: AVRT, including Wolff-Parkinson-White syndrome（WPW）

Conditions

  • AVRT, AVNRT

Interventions

DEVICE

THERMOCOOL SMARTTOUCH® Diagnostic/Ablation Deflectable Tip Catheter

THERMOCOOL SMARTTOUCH® catheter is a pressure catheter irrigated with cold saline, contact force sensing catheter. When used with Carto ®3 system, this catheter can provide a real time measurement for contact force. The magnitude and direction of the contact force can be displayed visually in the form of vector arrow on the top of catheter in Carto®3 system. It can be used for electrophysiological mapping and ablation of the heart.

Sponsors & Collaborators

  • Johnson & Johnson Medical (Shanghai) Ltd.

    lead INDUSTRY

Principal Investigators

  • Changsheng Ma, Professor · Beijing Anzhen Hospital

  • Haixiong Wang, Professor · Shanxi Cardiovascular Hospital

  • Shanglang Cai, Professor · The Affiliated Hospital of Qingdao University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-20
Primary Completion
2021-12-03
Completion
2021-12-14
FDA Device
Yes

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 NCT04923815 on ClinicalTrials.gov