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Evaluate the Efficiency Impact of Conducting Active Temperature Management During Cardiac Cryoablation Procedures

Evaluate the Efficiency Impact of Conducting Active Temperature Management During Cardiac Cryoablation Procedures

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04087122
Enrollment
20
Registered
2019-09-12
Start date
2019-09-30
Completion date
2020-12-31
Last updated
2022-05-12

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

Conditions

Atrial Fibrillation

Brief summary

Left atrial catheter ablation including pulmonary vein isolation is a standard therapy in the management of symptomatic atrial fibrillation; however thermal esophageal injury is a known potential consequence of this procedure. Delivery of radiofrequency (RF) energy necessary to perform left atrial ablation has the potential to cause injury to the nearby esophagus including ulceration, hematoma, spasm, esophageal motility disorders, and, in the most extreme case, atrial-esophageal fistula.Esophageal mucosal lesions are the likely precursor to AEF, and esophageal mucosal lesions have been detected on post-ablation endoscopy after pulmonary vein isolation with an incidence ranging from 3% to 60%. Active esophageal cooling during RF ablation as a means of esophageal injury prevention has been investigated through mathematical models, pre-clinical studies, and in clinical trials. Existing data support the efficacy of this approach, but the practice has not been widely adopted due to lack of a commercially available device. The aim of this study is to evaluate the impact on procedural efficiency of ablation procedures performed using esophageal heat transfer to warm the esophagus during left atrial cryoablation.

Detailed description

This study is a prospective, pilot study using the Attune Medical ensoETM esophageal heat transfer device to actively warm the esophagus during cryoablation procedures. This design is appropriate to gather the data needed regarding overall procedural time, compare this to historical controls, and estimate a sample size for a larger study powered for statistical significance. Once patient consent is obtained, the subject will undergo preparation and anesthesia procedures following standard practice. Once the patient is intubated, the esophageal heat transfer device will be placed into the esophagus according to the IFU. The device will remain in place until the ablation procedure is completed and will be removed before extubation. Left atrial cryoablation using the standard approach will be performed with the ensoETM set at a temperature of 42 degrees C. All patients will be followed up in total for 6 weeks (Long Term FU visit) after the procedure to document any clinical complication related to thermal esophageal injuries if applicable.

Interventions

DEVICEEsophageal warming device (Attune Medical, Chicago, IL

Prospective, single center pilot stud

Sponsors

Winchester Medical Center
CollaboratorOTHER
Advanced Cooling Therapy, Inc., d/b/a Attune Medical
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Adult patients (age over 18 years). * Undergoing cryoablation for the treatment of atrial fibrillation, including pulmonary vein isolation. * Patients must be able to understand and critically review the informed consent form. * Subjects must understand and agree to study requirements and sign a written informed consent.

Exclusion criteria

* Patients who are unable to provide informed consent. * Significant co-morbidities that preclude standard ablation procedure. * Patients with \<40 kg of body mass. * Patients with relevant esophageal pathology (e.g. esophageal cancer).

Design outcomes

Primary

MeasureTime frameDescription
Total Time of Active Ablation ProcedureStudy Day 1 for all patients enrolled, during left atrial ablation procedures using cryoablationTotal time of active ablation procedure measured from trans-septal puncture to achievement of Pulmonary Vein Isolation (PVI)

Secondary

MeasureTime frameDescription
Total Procedure TimeStudy Day 1 for all patients enrolled from patient entry to Electrophysiology (EP) lab until post procedure discharge to Post-Anesthesia Care Unit (PACU)]Total procedure time from patient entry to Electrophysiology (EP) lab until discharge to Post-Anesthesia Care Unit (PACU)
Number of Procedural Pauses During Left Atrial InstrumentationStudy Day 1 for all patients, during left atrial ablation procedures using cryoablationNumber of procedural pauses during left atrial instrumentation measured from trans-septal puncture to achievement of Pulmonary Vein Isolation (PVI)
Total Duration of Fluoroscopy UseStudy Day 1 for all patients, during left atrial ablation procedures using cryoablationTotal duration of fluoroscopy use during left atrial instrumentation measured from trans-septal puncture to achievement of Pulmonary Vein Isolation (PVI)

Countries

United States

Participant flow

Participants by arm

ArmCount
Esophageal Warming
Patients receive the Attune Medical Esophageal Heat Transfer Device
20
Total20

Baseline characteristics

CharacteristicEsophageal Warming
Age, Continuous68.5 years
STANDARD_DEVIATION 8.4
Race and Ethnicity Not Collected— Participants
Sex: Female, Male
Female
11 Participants
Sex: Female, Male
Male
9 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
0 / 20
other
Total, other adverse events
0 / 20
serious
Total, serious adverse events
0 / 20

Outcome results

Primary

Total Time of Active Ablation Procedure

Total time of active ablation procedure measured from trans-septal puncture to achievement of Pulmonary Vein Isolation (PVI)

Time frame: Study Day 1 for all patients enrolled, during left atrial ablation procedures using cryoablation

ArmMeasureValue (MEAN)
Esophageal WarmingTotal Time of Active Ablation Procedure126 minutes
Secondary

Number of Procedural Pauses During Left Atrial Instrumentation

Number of procedural pauses during left atrial instrumentation measured from trans-septal puncture to achievement of Pulmonary Vein Isolation (PVI)

Time frame: Study Day 1 for all patients, during left atrial ablation procedures using cryoablation

ArmMeasureValue (MEAN)
Esophageal WarmingNumber of Procedural Pauses During Left Atrial Instrumentation0 Procedural pauses
Secondary

Total Duration of Fluoroscopy Use

Total duration of fluoroscopy use during left atrial instrumentation measured from trans-septal puncture to achievement of Pulmonary Vein Isolation (PVI)

Time frame: Study Day 1 for all patients, during left atrial ablation procedures using cryoablation

ArmMeasureValue (MEAN)Dispersion
Esophageal WarmingTotal Duration of Fluoroscopy Use23.4 minutesStandard Deviation 7.8
Secondary

Total Procedure Time

Total procedure time from patient entry to Electrophysiology (EP) lab until discharge to Post-Anesthesia Care Unit (PACU)

Time frame: Study Day 1 for all patients enrolled from patient entry to Electrophysiology (EP) lab until post procedure discharge to Post-Anesthesia Care Unit (PACU)]

ArmMeasureValue (MEAN)
Esophageal WarmingTotal Procedure Time126 minutes

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