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Efficacy and Safety of the Sync-AV II Temporary Cardiac Pacing Catheter

NCT06261788 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-02-15

No results posted yet for this study

Summary

This is a prospective, single-center, non-randomized open label study. The objective of this study is to evaluate the efficacy and safety of the Sync-AV II Temporary Cardiac Pacing Catheter in subjects whose elective surgical or interventional procedure require temporary pacing support.

Conditions

  • Heart Block
  • Valve Heart Disease

Interventions

DEVICE

Temporary pacing

Transvenous temporary cardiac pacing - right internal jugular insertion

Sponsors & Collaborators

  • Regulatory and Quality Solutions

    collaborator UNKNOWN

  • Swift Sync, Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-06-01
Primary Completion
2023-09-13
Completion
2023-09-26

Countries

  • Paraguay

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 NCT06261788 on ClinicalTrials.gov