Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12618001815257
Ethics application status
Approved
Date submitted
29/10/2018
Date registered
7/11/2018
Date last updated
7/11/2018
Date data sharing statement initially provided
7/11/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Application of Decrement-Evoked Potential (DEEP) mapping during Atrial Fibrillation Ablation
Scientific title
An observational study of Decrement-Evoked Potential (DEEP) mapping during standard Atrial Fibrillation Ablation to establish feasibility and predictive power for Atrial Fibrillation Recurrence
Secondary ID [1] 296447 0
None.
Universal Trial Number (UTN)
Trial acronym
Atrial DEEP
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Atrial Fibrillation 310223 0
Condition category
Condition code
Cardiovascular 308956 308956 0 0
Other cardiovascular diseases

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
The study procedure involves the addition of pacing manoeuvres to map additional potentials called Decrement Evoked Potentials (DEEP), during standard procedures for ablation of persistent AF in patients who are clinically referred for an AF ablation procedure. The feasibility of delivering this pacing and measuring responses in atrial tissue will be tested, the relationship of DEEP areas to areas of scar and other signal abnormalities on voltage and activation mapping established (DEEP has recently shown promise in guiding ventricular tachycardia ablation) and the ability of DEEP to predict which patients will have AF recurrence explored. Pacing will be delivered at the end of the procedure by the electrophysiologist, after pulmonary vein isolation ablation, and will be with a drive train (S1=500ms) and extra stimulus (S2) at atrial Effective Refractory Period + 20ms, from specific protocol-specified sites in the left atrium. These include the left atrial appendage, roof, inferior-posterior wall, superior-posterior wall, anterior wall, mitral isthmus, high septum, low septum and inferior left atrium. Pacing for DEEP mapping will occur during the standard post-ablation waiting time, and will be additional to the usual ablation procedure, but will result in minimal additional procedural time compared to standard AF ablation. All analysis of DEEP will be performed offline post-procedure. Follow-up duration will be 12 months.
Intervention code [1] 312772 0
Diagnosis / Prognosis
Comparator / control treatment
No control group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 307921 0
Feasibility of DEEP mapping in the atrium during atrial fibrillation ablation procedure - ability to perform effectively with adequate signal quality to interpret results with reference to known DEEP parameters. Signal quality and reproducibility of electrograms will be assessed for consistency and signal-to-noise ratio and consensus from investigators obtained as to whether quality is adequate for interpretation and future application.
Timepoint [1] 307921 0
At initial AF ablation procedure.
Primary outcome [2] 307922 0
Clinical Recurrence of Atrial Fibrillation as detected on follow-up holter monitor or 12-lead ECG.
Timepoint [2] 307922 0
End of study follow-up (12 months).
Secondary outcome [1] 353355 0
Relationship of DEEP mapping abnormalities (location and area involved) to abnormal voltage on standard voltage mapping during atrial fibrillation ablation procedure.
Timepoint [1] 353355 0
At initial AF ablation procedure.
Secondary outcome [2] 353359 0
Relationship of DEEP mapping abnormalities (location and area involved) to abnormal activation patterns (for example complex fractionated atrial electrograms or re-entrant activity) on activation mapping during atrial fibrillation ablation procedure.
Timepoint [2] 353359 0
At initial AF ablation procedure.

Eligibility
Key inclusion criteria
Recurrent Atrial Fibrillation ablation, referred for catheter ablation.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Unable to provide informed consent.
Pregnant women.

Study design
Purpose
Natural history
Duration
Longitudinal
Selection
Defined population
Timing
Prospective
Statistical methods / analysis
Mean values and SDs will be calculated for normally distributed continuous variables; median and interquartile range for non-parametric data. Categorical data expressed will be expressed as percentages (ratio). Categorical data will be compared with a Fisher exact test or a chi-square test. Continuous data will be compared with the Student t test. A p value of <.05 will be considered significant. Kaplan-Meier curves for event-free survival will be constructed using the time to first AF recurrence. Comparison between both groups will be performed by log-rank statistics. Fifteen participants will be recruited from each of 5 international centres, giving 75 in total.

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
13/11/2018
Actual
Date of last participant enrolment
Anticipated
10/04/2019
Actual
Date of last data collection
Anticipated
10/04/2020
Actual
Sample size
Target
75
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 12296 0
John Hunter Hospital - New Lambton
Recruitment hospital [2] 12297 0
Lake Macquarie Private Hospital - Gateshead
Recruitment postcode(s) [1] 24488 0
2305 - New Lambton
Recruitment postcode(s) [2] 24489 0
2290 - Gateshead
Recruitment outside Australia
Country [1] 20978 0
United Kingdom
State/province [1] 20978 0
London
Country [2] 20979 0
Iceland
State/province [2] 20979 0
Reykjavik
Country [3] 20980 0
Canada
State/province [3] 20980 0
Toronto
Country [4] 20981 0
Spain
State/province [4] 20981 0
Madrid

Funding & Sponsors
Funding source category [1] 301043 0
Hospital
Name [1] 301043 0
John Hunter Hospital Cardiology Department
Country [1] 301043 0
Australia
Primary sponsor type
Hospital
Name
John Hunter Hospital Cardiology Department
Address
Level 3, John Hunter Hospital, Lookout Road, New Lambton, NSW 2305
Country
Australia
Secondary sponsor category [1] 300640 0
None
Name [1] 300640 0
Address [1] 300640 0
Country [1] 300640 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 301798 0
Hunter New England Human Research Ethics Committee
Ethics committee address [1] 301798 0
Ethics committee country [1] 301798 0
Australia
Date submitted for ethics approval [1] 301798 0
20/06/2018
Approval date [1] 301798 0
26/10/2018
Ethics approval number [1] 301798 0
18/06/20/3.01

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 88142 0
Dr Nicholas Jackson
Address 88142 0
John Hunter Hospital Cardiology department, Lookout Road, New Lambton. NSW. 2305.
Country 88142 0
Australia
Phone 88142 0
+61 2 49213000
Fax 88142 0
Email 88142 0
njackson193@gmail.com
Contact person for public queries
Name 88143 0
Nicholas Jackson
Address 88143 0
John Hunter Hospital Cardiology department, Lookout Road, New Lambton. NSW. 2305.
Country 88143 0
Australia
Phone 88143 0
+61 2 49213000
Fax 88143 0
Email 88143 0
njackson193@gmail.com
Contact person for scientific queries
Name 88144 0
Nicholas Jackson
Address 88144 0
John Hunter Hospital Cardiology department, Lookout Road, New Lambton. NSW. 2305.
Country 88144 0
Australia
Phone 88144 0
+61 2 49213000
Fax 88144 0
Email 88144 0
njackson193@gmail.com

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Undecided
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.