Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to validate a novel method of diagnosing arrhythmias using the NAVA catheter-positioning screen in patients who have a NAVA catheter in place.


Clinical Trial Description

The population will be a convenience sample of adults with various arrhythmias who are scheduled to undergo an electrophysiology study and-or ablation (EPSA) under general anesthesia (GETA) at The Toledo Hospital.

After the patient has been successfully intubated at the beginning of the procedure, a trained nurse, using standard technique for placement of a oro/nasogastric tube, will place an appropriately sized NAVA catheter in the patient. The lumen of the NAVA tube can be used as a conventional oro/nasogastric tube and the electrodes will be connected to the Servo-I ventilator. Although the Servo-I is a ventilator, it will be used only as a monitor for this study. The position of the nasogastric tube will then be refined using the catheter positioning screen as needed.

During the course of the EPSA various arrhythmias may become evident. When these are noted, screen shots will be saved on the Servo-i monitor. Surface and electrogram recordings will be saved at the same time. The NAVA catheter will be disconnected from the Servo-I monitor during the ablation part of the procedure to prevent inadvertent damage to the monitor. ;


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02040675
Study type Observational
Source ProMedica Health System
Contact
Status Completed
Phase N/A
Start date February 2014
Completion date March 2016

See also
  Status Clinical Trial Phase
Completed NCT05067114 - Solutions for Atrial Fibrillation Edvocacy (SAFE)
Completed NCT02241252 - Using an iPhone ECG to Monitor the QT Interval on Dofetilide and Sotalol Patients N/A
Completed NCT01428778 - Berlin Beat of Running Study N/A
Completed NCT01626261 - Examination of Implant´s Safety in an Electronic and Magnetic Field Environment
Withdrawn NCT01359683 - Heart Rate Variability Changes During Cardiac Surgery And The Incidence Of Post-Operative Cardiac Arrhythmias N/A
Recruiting NCT04154982 - N-Acetylcysteine Protection Against Radiation Induced Cellular Damage Phase 2
Completed NCT04609683 - Measuring Hydration Levels of Healthy and Heart Failure Patients Before, During, and After an Electrophysiology (EP) Procedure N/A
Completed NCT04162249 - High Radiofrequency Power for Faster and Safer Pulmonary Veins Isolation - a Pilot Observational Study.
Withdrawn NCT05084391 - Phase I/II Randomized Study of Stereotactic Ablative Radiotherapy (SABR) Versus Standard of Care for Refractory Structural Cardiac Arrhythmias (SABR-HEART) Phase 1/Phase 2
Completed NCT03260244 - EnSite Precision Observational Study
Recruiting NCT04474418 - Psychometric Characterization of Patients With Cardiac Arrhythmias
Recruiting NCT03996954 - Validation of a Smartphone-based Recorder for Detection of Cardiac Arrhythmias N/A
Recruiting NCT05508880 - SIGIL: Signal Interpretation and Analysis In Real Life Cardiac Arrhythmias
Terminated NCT04552665 - Prospective Procedural Data Collection for Continuous Improvement of the KODEX - EPD™ System Performance.
Recruiting NCT06073509 - Atrial Fibrillation and Other Cardiac Arrhythmias and Diseases After Radiotherapy for Breast Cancer : Watch Your HeaRT
Completed NCT04463524 - Screening for Hearth Rhythm Disorders
Withdrawn NCT01394965 - Electrocardiographic Mapping and Imaging Phase 0
Completed NCT01672528 - Patient Reported Outcome Measures for Ablation of Cardiac Arrhythmias
Completed NCT02232204 - Sleep and Ventricular Arrhythmias Study Phase 2
Completed NCT05114382 - An Evaluation of the Safety and Performance of the CathVision Cube® System N/A