Ignite Creation Date:
2024-05-06 @ 3:15 PM
Last Modification Date:
2024-10-26 @ 1:46 PM
Study NCT ID:
NCT04577859
Status:
RECRUITING
Last Update Posted:
2024-06-20
First Post:
2020-09-30
Brief Title:
Esophageal Protection Study A Multicenter Study
Sponsor:
Advanced Cooling Therapy Inc dba Attune Medical
Organization:
Advanced Cooling Therapy Inc dba Attune Medical
Study Overview
Official Title:
Improving Esophageal Protection During AF Ablation a Multicenter Double-blind Randomized Clinical Trial
Status:
RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
eCool-US
Brief Summary:
Atrial fibrillation AF is a common debilitating heart rhythm condition that can cause heart failure and negatively impact a patients outlook in terms of symptoms and disability It is an irregular fast heart rhythm disorder coming from the top chamber of the heart left atrium Catheter ablation treatment has been shown to be effective in controlling or eliminating AF and its associated symptoms This is now a common and effective treatment option for patients suffering with AF During ablation thermal energy is applied in the top chamber of the heart the left atrium to abolish abnormal electrical signals that cause AF It is generally a safe procedure but one potential risk associated with this procedure is damage to the esophagus caused by thermal energy being transmitted to the esophagus from the heart The esophagus sits just behind the heart chamber where ablation work is performed about 5mm away so it is vulnerable to damage Although the risk of severe esophageal damage is low if it occurs it can be serious as the patient may become very ill as a result
In recent studies it was shown that a more advanced type of esophageal probe ensoETM that cools the esophagus during ablation is better at protecting the esophagus from ablation-related injury compared to the standard care temperature monitoring probe currently used The ensoETM is a CE marked and FDA-cleared device with an intended purpose of controlling patient temperature and has received marketing authorization from FDA to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures
The purpose of this study is to determine if the long-term efficacy outcome results obtained in single pilot studies can be replicated in a prospective multi-center randomized controlled trail comparing the the esophageal cooling probe versus a standard of care esophageal temperature monitoring probe There is a 5050 chance of the esophageal cooling probe being used during AF ablation for participants
In recent studies it was shown that a more advanced type of esophageal probe ensoETM that cools the esophagus during ablation is better at protecting the esophagus from ablation-related injury compared to the standard care temperature monitoring probe currently used The ensoETM is a CE marked and FDA-cleared device with an intended purpose of controlling patient temperature and has received marketing authorization from FDA to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures
The purpose of this study is to determine if the long-term efficacy outcome results obtained in single pilot studies can be replicated in a prospective multi-center randomized controlled trail comparing the the esophageal cooling probe versus a standard of care esophageal temperature monitoring probe There is a 5050 chance of the esophageal cooling probe being used during AF ablation for participants
Detailed Description:
The purpose of this research project is to investigate if the long-term efficacy outcome freedom from arrythmia when using an esophageal cooling probe is potentially better than a standard of care temperature monitoring probe This is the multi-center study is being done to confirm single center study results showing better long term efficacy This study will also add to existing data showing reductions in esophageal injury with optional EGDs
At present the method of protection is limited an esophageal temperature monitoring probe is inserted whilst the patient is under general anesthesia and the temperature is measured during ablation stopping if temperatures markedly increase which may suggest significant esophageal thermal injury This method is unreliable as the temperature probe does not sit well in the esophagus and is often too far away from the area requiring monitoring The probe is difficult to place as it can coil
The esophageal cooling device ensoETM is another protection method that is gaining popularity since receiving marketing authorization from FDA to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures While the acute safety data has been accepted long-term efficacy outcomes improvements with use of ensoETM has not been confirmed outside of single center randomized studies
The design of the project is in the form of a randomized controlled trial like the single-center studies so participants will have a 5050 chance of being allocated to the study group receiving the esophageal cooling probe ensoETM or to the control group receiving the esophageal temperature monitoring probe
The patient is blinded to the result of the randomization to avoid biasplacebo effect
If enrolled to the study group the esophageal cooling probe ensoETM will be used This is a smooth medical-grade silicone multi-lumen esophageal probe the device has a CE mark and FDA clearance and is designed for the purpose of esophageal insertion and temperature management that allows water irrigation in a closed loop system when connected to an external console If the console cools the irrigated water this is controlled by manual updown buttons depending on what temperature is desired the esophageal probe is then cooled also which allows local esophageal wall temperature to be controlled Esophageal cooling via the ensoETM probe can then counteract any transmitted thermal energy from the ablation The ensoETM has already received marketing authorization from FDA to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures
The ablation procedure is normally done under general anesthetic so the participant will not be aware of what group they are assigned and will not be subjected to any sensation of pain or discomfort The ensoETM probes are soft and much gentler than the camera probe that the team normally have to insert during the catheter ablation procedure the camera probe or transesophageal echocardiography TEE- is part of standard care so the study authors are of the opinion that this additional precautionary measure does not itself increase the patients risk or exposure to harm
After the procedure participants study or control may have an optional endoscopy camera between 12-72 hours after the catheter ablation procedure to review for degree of esophageal thermal damage caused by ablation if any The endoscopist is also blinded to the result of the randomization to avoid bias during reporting of the endoscopy result The short time window between ablation and endoscopy camera follow up means that it can be done at the same admission as the ablation procedure itself this is advantageous for the patient as both the ablation treatment and the follow up camera can be completed in 1 hospital admission The endoscopy camera result is explained to the patient on the day and if any further action required
After this normalstandard care clinic follow up of the patient will be adhered to but as part of the trial at the first clinic follow up participants in both groups will be asked about any lingering gastro-esophageal symptoms and a record is made of this for the study The patient is still blinded to the results of the randomization at the time of reporting their symptoms during recovery if any This is to avoid biasplacebo effect
The research project does not create any areas of ethical concern as the soft esophageal cooling deviceprobe is of gentle design specifically made to sit in the esophagus Especially when compared to the TOE probe that is normally used as part of standard protocol for an AF ablation procedure The patient will also not be aware of this step at all as the procedure is conducted under general anesthesia The device is appropriately CE marked and FDA cleared for the indication of body cooling via the esophagus and with marketing authorization to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures Even in standard care an esophageal temperature monitoring probe is required so effectively this study simply randomizes the patient to either the esophageal cooling probe or another standard of care probe during their AF ablation
There is one additional optional follow up the participant may have as part of this trial the endoscopy camera regardless of if randomized to study or control group The endoscopy camera will be completed by 12-72hrs post catheter ablation procedure The purpose is to review any areas of inflammation or thermal injury in the esophagus that may alter clinical management but this specific information will also be used during study analysis of the 2 randomized groups after the study has completed An endoscopy camera is considered to be a low risk outpatient procedure that takes 20 minutes to complete The risk of this camera test causing any damage itself is 05 A TEE probeany other esophageal probe used during the ablation procedure is similar to the endoscopy probe so apart from the participant attending an additional optional appointment after their ablation the overall risk to the patient is not significantly increased
The follow up endoscopy camera may be slightly uncomfortable in the beginning but it is not painful is straightforward and relatively quick- this will be explained in the beginning during the recruitment process so the potential participant has an accurate idea of what to expect from the endoscopy camera if they choose to get this procedure There is added benefit to the patient from this follow up as the endoscopy camera will confirm to the patient about any esophageal injury from ablation and if any treatment is required If no injury this can help to reassure the patient before they go home
Lastly the follow up clinics will be as normal for the participant only that investigators will ask specifically for any ongoing gastroesophageal symptoms as well A record of this will be made
The study authors reviewed the steps involved with this study design and concluded that no major ethical or legal issue has been identified The summary of the steps involved here hopefully clarifies our viewpoint From a management perspective the centers involved are able to conduct catheter ablation procedures for AF with general anesthetic The authors have experience and acquired the necessary equipment from the esophageal cooling device company and have appropriate device management protocols and storage space in place The endoscopy department at the participating centers are also equipped to support additional follow up with endoscopy tests post ablation
Lastly the proposed research trial has been similarly conducted in single-site settings to great success and with excellent safety record with no probe-related trauma and the team did not encounter any new or unexpected issues or difficulties The authors obtained good patient feedback from the single-center studies This same trial will run at 5 or more sites across the US with potential to further expand depending on statistical analysis
At present the method of protection is limited an esophageal temperature monitoring probe is inserted whilst the patient is under general anesthesia and the temperature is measured during ablation stopping if temperatures markedly increase which may suggest significant esophageal thermal injury This method is unreliable as the temperature probe does not sit well in the esophagus and is often too far away from the area requiring monitoring The probe is difficult to place as it can coil
The esophageal cooling device ensoETM is another protection method that is gaining popularity since receiving marketing authorization from FDA to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures While the acute safety data has been accepted long-term efficacy outcomes improvements with use of ensoETM has not been confirmed outside of single center randomized studies
The design of the project is in the form of a randomized controlled trial like the single-center studies so participants will have a 5050 chance of being allocated to the study group receiving the esophageal cooling probe ensoETM or to the control group receiving the esophageal temperature monitoring probe
The patient is blinded to the result of the randomization to avoid biasplacebo effect
If enrolled to the study group the esophageal cooling probe ensoETM will be used This is a smooth medical-grade silicone multi-lumen esophageal probe the device has a CE mark and FDA clearance and is designed for the purpose of esophageal insertion and temperature management that allows water irrigation in a closed loop system when connected to an external console If the console cools the irrigated water this is controlled by manual updown buttons depending on what temperature is desired the esophageal probe is then cooled also which allows local esophageal wall temperature to be controlled Esophageal cooling via the ensoETM probe can then counteract any transmitted thermal energy from the ablation The ensoETM has already received marketing authorization from FDA to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures
The ablation procedure is normally done under general anesthetic so the participant will not be aware of what group they are assigned and will not be subjected to any sensation of pain or discomfort The ensoETM probes are soft and much gentler than the camera probe that the team normally have to insert during the catheter ablation procedure the camera probe or transesophageal echocardiography TEE- is part of standard care so the study authors are of the opinion that this additional precautionary measure does not itself increase the patients risk or exposure to harm
After the procedure participants study or control may have an optional endoscopy camera between 12-72 hours after the catheter ablation procedure to review for degree of esophageal thermal damage caused by ablation if any The endoscopist is also blinded to the result of the randomization to avoid bias during reporting of the endoscopy result The short time window between ablation and endoscopy camera follow up means that it can be done at the same admission as the ablation procedure itself this is advantageous for the patient as both the ablation treatment and the follow up camera can be completed in 1 hospital admission The endoscopy camera result is explained to the patient on the day and if any further action required
After this normalstandard care clinic follow up of the patient will be adhered to but as part of the trial at the first clinic follow up participants in both groups will be asked about any lingering gastro-esophageal symptoms and a record is made of this for the study The patient is still blinded to the results of the randomization at the time of reporting their symptoms during recovery if any This is to avoid biasplacebo effect
The research project does not create any areas of ethical concern as the soft esophageal cooling deviceprobe is of gentle design specifically made to sit in the esophagus Especially when compared to the TOE probe that is normally used as part of standard protocol for an AF ablation procedure The patient will also not be aware of this step at all as the procedure is conducted under general anesthesia The device is appropriately CE marked and FDA cleared for the indication of body cooling via the esophagus and with marketing authorization to reduce the likelihood of ablation-related esophageal injury resulting from radiofrequency cardiac ablation procedures Even in standard care an esophageal temperature monitoring probe is required so effectively this study simply randomizes the patient to either the esophageal cooling probe or another standard of care probe during their AF ablation
There is one additional optional follow up the participant may have as part of this trial the endoscopy camera regardless of if randomized to study or control group The endoscopy camera will be completed by 12-72hrs post catheter ablation procedure The purpose is to review any areas of inflammation or thermal injury in the esophagus that may alter clinical management but this specific information will also be used during study analysis of the 2 randomized groups after the study has completed An endoscopy camera is considered to be a low risk outpatient procedure that takes 20 minutes to complete The risk of this camera test causing any damage itself is 05 A TEE probeany other esophageal probe used during the ablation procedure is similar to the endoscopy probe so apart from the participant attending an additional optional appointment after their ablation the overall risk to the patient is not significantly increased
The follow up endoscopy camera may be slightly uncomfortable in the beginning but it is not painful is straightforward and relatively quick- this will be explained in the beginning during the recruitment process so the potential participant has an accurate idea of what to expect from the endoscopy camera if they choose to get this procedure There is added benefit to the patient from this follow up as the endoscopy camera will confirm to the patient about any esophageal injury from ablation and if any treatment is required If no injury this can help to reassure the patient before they go home
Lastly the follow up clinics will be as normal for the participant only that investigators will ask specifically for any ongoing gastroesophageal symptoms as well A record of this will be made
The study authors reviewed the steps involved with this study design and concluded that no major ethical or legal issue has been identified The summary of the steps involved here hopefully clarifies our viewpoint From a management perspective the centers involved are able to conduct catheter ablation procedures for AF with general anesthetic The authors have experience and acquired the necessary equipment from the esophageal cooling device company and have appropriate device management protocols and storage space in place The endoscopy department at the participating centers are also equipped to support additional follow up with endoscopy tests post ablation
Lastly the proposed research trial has been similarly conducted in single-site settings to great success and with excellent safety record with no probe-related trauma and the team did not encounter any new or unexpected issues or difficulties The authors obtained good patient feedback from the single-center studies This same trial will run at 5 or more sites across the US with potential to further expand depending on statistical analysis
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
True
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None