Comparison of Treatment of Atrial Fibrillation (AF) Between Surgical Ultrasonic Technology or Drug Therapy for Patients With AF Requiring Mitral Valve Surgery (EPICAF)
Primary Purpose
Mitral Valvulopathy, Atrial Fibrillation
Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
EPICOR
Amiodarone
Sponsored by
About this trial
This is an interventional treatment trial for Mitral Valvulopathy focused on measuring Mitral valvulopathy, Atrial Fibrillation, Amiodarone, Paroxysmal Atrial Fibrillation, Chronic Atrial Fibrillation, Ultrasound Technique
Eligibility Criteria
Inclusion Criteria:
- mitral valvulopathy requiring surgery
- paroxysmal atrial fibrillation or permanent or chronic atrial fibrillation
- Left atrium ≤ 55mm
- consent form signed
Exclusion Criteria:
- thyroid dysfunction
- pregnant
- contraindication of amiodarone
Sites / Locations
- CHU de Grenoble
- Hospices Civiles de Lyon
- CHU de Montpellier
- CHU de Rennes
- CHU de Saint-Etienne
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
EPICOR
Amiodarone
Arm Description
Cardiac ablation system EPICOR (CE n°0344). ablation device EpicorTM UltraCinchTM LP (Class III device) Positioning system and calibration EpicorTM LP (LP PASTM; device Class IIa) Cable connection EpicorTM LP (unsterile) Ablation Control System EpicorTM LP (Class IIb)
Cordarone : 400 mg/d during the 2 first months 200 mg/d from 3th to 18th month
Outcomes
Primary Outcome Measures
Atrial Fibrillation episode
At least one episode of symptomatic AF or asymptomatic sustained [> 10 minutes] documented by an ECG or an R-test changes, occurring between 3 months (after restoration of sinus rhythm by cardioversion if necessary at the end of the 2nd month) and 18th month
Secondary Outcome Measures
Adverse drug effects of Amiodarone
side effects attributable to treatment with amiodarone and has caused it to stop
major cardiovascular event
An atrial arrhythmia or heart failure or embolic events
Atrial tachycardia
Atrial tachycardia whose frequency is between 150 and 250 per minute and shows the appearance of which electrocardiographic waves P positive on D2, D3 and AVF.
Death
Full Information
NCT ID
NCT01649544
First Posted
July 23, 2012
Last Updated
November 30, 2015
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Ministry of Health, France
1. Study Identification
Unique Protocol Identification Number
NCT01649544
Brief Title
Comparison of Treatment of Atrial Fibrillation (AF) Between Surgical Ultrasonic Technology or Drug Therapy for Patients With AF Requiring Mitral Valve Surgery
Acronym
EPICAF
Official Title
Comparison of Treatment of Atrial Fibrillation (AF) Between Surgical Ultrasonic Technology (EPICOR) or Drug Therapy (Cordarone) for Patients With AF Requiring Mitral Valve Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
November 2015
Overall Recruitment Status
Terminated
Why Stopped
End of commercialization of the medical device
Study Start Date
March 2012 (undefined)
Primary Completion Date
September 2015 (Actual)
Study Completion Date
September 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Ministry of Health, France
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
In pre-operative cardiac surgery, 30 to 40% of patients with mitral valvulopathy have had episodes of paroxysmal atrial fibrillation (PAF) or are in permanent or chronic atrial fibrillation (CAF). According to the 1999 PMSI data, close to 4000 mitral valve interventions were performed in France, in other words, more than 1000 patients present with this condition annually; despite a surgical correction of their valvulopathy, patients presenting with a pre-operative chronic atrial fibrillation remain in fibrillation following surgery despite treatment with anti-arrhythmic agents associated or not with a cardioversion. Thus, the survival rate without AF recurrence is 10% at 1 year and 5% at 2 years in patients with AF prior to surgery; on the other hand, patients in sinus rhythm at the time of surgery and without an antecedent of AF exhibit an incidence of no AF of 90% and 74% at 1 and 2 years, respectively. It has also been shown in numerous studies that the long-term morbidity in patients with atrial valve surgery is higher in those with AF.
For more than 10 years, radio-frequency techniques using the endocavitary approach have shown a greater efficacy in maintaining sinus rhythm than drug therapy even though the techniques are invasive. These radio-frequency techniques were developed and tested during mitral surgery, but, to the investigators knowledge, there is only one randomized study that was carried out in a population with permanent AF using radio-frequency technique via the endocardial approach. Maintenance of sinus rhythm was obtained in only 44.4% of patients versus 4.5% in the control group; these results are not in accordance with the published prospective and retrospective registries using the technique peri-operatively. The principal problem of this study is the absence of medical treatment in the control group. In addition, the use of the radio-frequency technique requires an atriotomy resulting in a prolonged surgical time, which increases the peri-operative morbidity.
Other simpler ablation techniques have been developed, such as the one using ultrasound. In comparison with the radio-frequency method, this latter technique presents numerous advantages including the absence of an atriotomy due to the fact that the epicardial pathway is used, a short procedure time (11 min on average), excellent reproducibility, the transmural character of the lesions, along with the simplicity of application. There is not, to the investigators knowledge, a randomized study comparing the peri-operative ultrasound technique (EPICOR) in mitral valve surgery with the conservative reference treatment, notably mitral valve surgery coupled with long-term amiodarone treatment. In effect, while amiodarone is the most efficacious anti-arrhythmic agent in the long-term, this drug is associated with a high percentage of significant side effects, close to 20% at 2 years. The only available results using the ultrasound technique are the registries pertaining to the follow-up of patients undergoing cardiac mitral or aortic surgery, with an antecedent of AF. The results appear to be encouraging with 85% of cases maintained in sinus rhythm at 12 months in the most recent studies. In this clinical context, a French multi-centric registry evaluated the peri-operative treatment of AF with all of the proposed techniques (cryotherapy, radio-frequency, and ultrasound). The percentage of maintenance of sinus rhythm appears to be lower than in the historical registries, at the level of 60%, but the techniques used in this registry were multiple even if 50% of patients were treated with ultrasound; in addition, there was no randomization and follow-up was only for 6 months.
Detailed Description
As a consequence, it is very difficult to have a precise idea, in the literature, of the medium- and long-term efficacy of this technique. Despite a diffusion and utilization of the technique in clinical practice, the efficacy of the ultrasound technique has not been compared, in a standardized manner, with amiodarone, which is the only anti-arrhythmic agent that has shown good efficacy in maintaining post-operative sinus rhythm following cardiac surgery. We propose to undertake an open, prospective, randomized, multicenter study evaluating the efficacy of treatment with ultrasound (EPICOR) in the maintenance of sinus rhythm following mitral surgery in two parallel groups, one group with ablation via ultrasound "EPICOR" and a control group treated with "amiodarone", including a long-term follow-up of 18 months. The strategy in this study necessitates the use of amiodarone in the two groups during the first 2 months followed by a cardioversion in the cases of persistent AF 2 months following surgery in both groups, with a cessation of amiodarone therapy in the ultrasound group and maintenance of therapy in the control group. The parallel treatment with amiodarone in the two groups following the surgical intervention is necessary in order to avoid confounding factors in the analysis. In effect, AF during the postoperative period is frequent and may be considered to be secondary to a number of factors, such as the surgery itself, inflammation, temperature, metabolic disturbances, pericardial effusion, etc. This approach is justified, because if the benefit associated with the peri-operative ultrasound technique is validated, this would allow for a reduction in the use of anti-arrhythmic agents, which are associated with side effects, along with a decrease in long-term morbidity via the resulting maintenance of sinus rhythm. In addition, the technique of ablation via ultrasound could, among others, replace the surgical technique of reference (Cox surgery) for which the principal inconvenience is the prolongation of the time of surgery, resulting in an elevated peri-operative morbidity. Therefore, the principal objective of the study is to compare, at 18 months, the efficacy of surgical treatment with ultrasound (EPICOR) on the maintenance of sinus rhythm following mitral valve surgery in comparison with amiodarone.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mitral Valvulopathy, Atrial Fibrillation
Keywords
Mitral valvulopathy, Atrial Fibrillation, Amiodarone, Paroxysmal Atrial Fibrillation, Chronic Atrial Fibrillation, Ultrasound Technique
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
6 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EPICOR
Arm Type
Experimental
Arm Description
Cardiac ablation system EPICOR (CE n°0344).
ablation device EpicorTM UltraCinchTM LP (Class III device)
Positioning system and calibration EpicorTM LP (LP PASTM; device Class IIa)
Cable connection EpicorTM LP (unsterile)
Ablation Control System EpicorTM LP (Class IIb)
Arm Title
Amiodarone
Arm Type
Active Comparator
Arm Description
Cordarone :
400 mg/d during the 2 first months 200 mg/d from 3th to 18th month
Intervention Type
Device
Intervention Name(s)
EPICOR
Intervention Description
Intraoperatively, in addition to the usual gesture, it will be conducted a systematic exclusion-ligation of the left atrium and the establishment of electrodes atrial and ventricular pacing. The right pulmonary veins are isolated by dissection of the inter-atrial groove and application of the probe by biting on the atrial tissue, the procedure is identical on the left after dissection of the area between the left pulmonary artery and pulmonary veins. The use of ultrasound application will require 10 minutes to around the pulmonary veins using a multi-electrode probe set to deliver an output pulse from 15 to 100 Watts at a frequency from 3.5 to 4.6 MHz. Using EPICOR extends the operating time of 15 minutes.
Intervention Type
Drug
Intervention Name(s)
Amiodarone
Primary Outcome Measure Information:
Title
Atrial Fibrillation episode
Description
At least one episode of symptomatic AF or asymptomatic sustained [> 10 minutes] documented by an ECG or an R-test changes, occurring between 3 months (after restoration of sinus rhythm by cardioversion if necessary at the end of the 2nd month) and 18th month
Time Frame
At 18 months
Secondary Outcome Measure Information:
Title
Adverse drug effects of Amiodarone
Description
side effects attributable to treatment with amiodarone and has caused it to stop
Time Frame
At 18 months
Title
major cardiovascular event
Description
An atrial arrhythmia or heart failure or embolic events
Time Frame
At 18 months
Title
Atrial tachycardia
Description
Atrial tachycardia whose frequency is between 150 and 250 per minute and shows the appearance of which electrocardiographic waves P positive on D2, D3 and AVF.
Time Frame
At 18 months
Title
Death
Time Frame
At 18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
mitral valvulopathy requiring surgery
paroxysmal atrial fibrillation or permanent or chronic atrial fibrillation
Left atrium ≤ 55mm
consent form signed
Exclusion Criteria:
thyroid dysfunction
pregnant
contraindication of amiodarone
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antoine DA COSTA, MD PhD
Organizational Affiliation
CHU de Saint-Etienne
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Grenoble
City
Grenoble
Country
France
Facility Name
Hospices Civiles de Lyon
City
Lyon
Country
France
Facility Name
CHU de Montpellier
City
Montpellier
Country
France
Facility Name
CHU de Rennes
City
Rennes
Country
France
Facility Name
CHU de Saint-Etienne
City
Saint-etienne
Country
France
12. IPD Sharing Statement
Learn more about this trial
Comparison of Treatment of Atrial Fibrillation (AF) Between Surgical Ultrasonic Technology or Drug Therapy for Patients With AF Requiring Mitral Valve Surgery
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