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Retracting the Esophagus During AF Ablation

Esophageal Stylet as a Strategy to Minimize the Risk of Esophageal Injury During the Atrial Fibrillation Catheter Ablation Procedure.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02665442
Acronym
EsoSure
Enrollment
40
Registered
2016-01-27
Start date
2016-01-31
Completion date
2018-01-31
Last updated
2016-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation, Cardiac Arrhythmia, Esophageal Fistula

Keywords

Esophageal Stylet, EsoSure, Atrial Fibrillation, Catheter Ablation, Mechanical esophageal displacement

Brief summary

This Study is designed to determine the outcome and effect of implementation of Esophageal Stylet as a strategy to minimize the risk of esophageal injury during the atrial fibrillation catheter ablation procedure.

Detailed description

There is a clear potential to produce transmural esophageal injury during catheter ablation for AF when employing a lesion set targeting the posterior left atrial wall and pulmonary vein (PV) antra using contemporary large-tip or irrigated-tip catheter ablation systems when endocardial target sites are in close proximity to the esophagus. It is very likely that a movement by the Esophageal Stylet of only 2 to 3 centimeters from the midline can safely protect the esophagus from thermal injury and will mimic the natural migration of the esophagus itself. The Stylet proposes to safely facilitate lateral esophageal movement in a manner consistent with the esophagus's own natural migration in order to displace and maintain the esophagus's position away from potential damage resulting from a cardiac ablation procedure in the left atrium or coronary sinus. The Esophageal Stylet is a thin rigid tube, which will be inserted inside a commonly used nasogastric tube placed inside the esophagus during the ablation. We will use this stylet to move the esophagus away from the site of the ablation about 1-2 centimeters. Other common procedures, such as (Trans-esophageal Echocardiogram), move the esophagus twice this distance with a low risk.

Interventions

DEVICEEsophageal Stylet - EsoSure

The Esophageal Stylet is a thin rigid tube, which will be inserted inside a commonly used nasogastric tube placed inside the esophagus during the ablation. We will use this stylet to move the esophagus away from the site of the ablation about 1-2 centimeters.

Sponsors

Northeast Scientific, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Age 18 or above for the Patient or legal representative to provide informed consent. 2. Documented paroxysmal or persistent Atrial Fibrillation by a Cardiologist and EKG finding. 3. The patient will undergo Atrial Fibrillation catheter ablation as a treatment plan.

Exclusion criteria

1. Bleeding disorder. 2. Dysphagia to solid and liquid or any documented esophageal masses or cancer. 3. Esophageal varices, diverticulum, esophageal web, upper GI bleeding, or hiatal hernia.

Design outcomes

Primary

MeasureTime frameDescription
Esophageal injury or erosion2-3 days post ablationDecrease of esophageal thermal injury detected by esophageal Pill-Cam

Secondary

MeasureTime frameDescription
Recurrence of Atrial Fibrillation12 MonthsDecrease of atrial fibrillation recurrence after 12 months
Total radiofrequency timeDay of ablation procedureDecrease the total time of radiofrequency ablation at the procedure time

Countries

United States

Contacts

Primary ContactMedhat Abdelmessih, MD
medhat.abdelmessih@yale.edu(203) 737-1330
Backup ContactDawn Shaddinger, MSN, CCRN
Dawn.Shaddinger@yale.edu(203) 737-3570

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026