- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03075930
Atrial Fibrillation Ablation Registry (AFAB)
A Registry With the Aim to Identify Characteristics of Atrial Conduction and Risk of Recurrence in Patients With Atrial Fibrillation Undergoing Ablation for Atrial Fibrillation
This is a single centre prospective data registry. In this study atrial conduction characteristics of extended surface Electrocardiograms (esECG), biomarkers and genetic analysis will be performed before ablation, before discharge and 3 months after catheter ablation of atrial fibrillation (AF) and compared to routine clinical follow-up data.
The objective of this registry is to establish a data registry of patients undergoing ablation of AF. Supplementary to the routine clinical diagnostic an esECG and an analysis of biomarkers will be performed and compared to clinical and outcome data.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Electro anatomical remodelling of the atria due to ageing or structural heart disease leads to AF which in turn leads to cardiac electrical and structural remodelling. In case of advanced remodelling restoration of sinus rhythm (SR) becomes more difficult and the results of catheter ablation are disappointing. Furthermore, there is no valid parameter to predict or diagnose recurrence of AF during SR after successful ablation, so repeated long-term electrocardiogram (ECG) recordings have to be performed to detect asymptomatic AF episodes in particular.
Thus, the rationale to establish a systematic review of patient data in a registry are:
- Self-termination AF leads to slight, persistent AF leads to more advanced cardiac remodelling, shown in altered atrial conduction properties
- Early recognition and therapy of AF improves the outcome, thus clinical parameter to predict or diagnose recurrence of AF during SR are desirable Ablation of AF is predominantely performed using standard endocardial transvenous technique of pulmonary veins isolation (PVI) by radiofrequency or cryoballoon ablation. For medical reasons specific ablation techniques like additional ablation lines or an epicardial approach is in discretion of the treating cardiologist. The esECG is measured by signal averaged routine 12-lead ECG with 3-5 supplementary leads before ablation, before discharge and 3 months after ablation. 2 tubes of EDTA plasma will be taken supplementary during routine venous puncture on admission and analysed for biomarkers and common gene variants.
During 5 years every participant receives an esECG before ablation, before discharge and three months after ablation. Routine follow-up data of each participant is included until 12 months of follow-up.
Patients who are included would also undergo a procedure without participation in this study. Risks (complications of procedures) are associated with the procedure and not with participation in the registry. The supplementary diagnostics performed for the registry are comprehensible to clinical routine ECG diagnostics. Extra (study-related) investigations consist of esECG (a signal averaged surface ECG with 3-5 supplementary leads at baseline before ablation), before discharge, and 3 months after ablation, and possibly also a body surface potential map (BSPM). These are always planned together with routine follow-up, no extra visits are necessary. The esECG and BSPM can be compared to regular ECGs, the only additional discomfort might be the number of leads. Furthermore 2 tubes of EDTA plasma blood will be taken supplementary at the routine admission venous puncture for further biomarker and common gene variants analysis.
Quality assurance plan: All data will be stored in 2 independent database. In the first database personal and contact informations are stored with a decent patient ID number in ascending order. In the other database all medical informations will be stored without personal data of the patient. The database has algorithm to prevent mesenteries and rudimentary checks for data integrity and consistency. List are provided for repeated parameters and all variables are explained if relevant. Standard operating procedures are provided for relevant steps in patient inclusion, measurements and data entry.
Because of the registry character no sample size calculation is provided yet. But after the first year of inclusion a data analysis will provide informations about an expected sample size. To date we calculate for an period of patient inclusion of 5 years.
Data inconsistency could not be avoided due to the registry character of this study and will marked in a respective way.
Statistical analysis will be performed after the first year of patients including logistic regression analysis to determine the discriminative power of the recorded ECG for the clinical outcome and recurrence of AF.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Matthias D Zink, Physician
- Phone Number: 00491797523510
- Email: m.zink@maastrichtuniversity.nl
Study Contact Backup
- Name: Ulrich Schotten, Physician
- Email: schotten@maastrichtuniversity.nl
Study Locations
-
-
Limburg
-
Maastricht, Limburg, Netherlands, 6229HX
- Recruiting
- Maastricht University
-
Contact:
- Matthias D Zink, Physician
- Phone Number: 00491797523510
- Email: m.zink@maastrichtuniversity.nl
-
Contact:
- Ulrich Schotten, Physician
- Email: schotten@maastrichtuniversity.nl
-
Principal Investigator:
- Matthias D Zink, Physician
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Documented self-terminating or persistent AF
- Scheduled for ablation of AF
- At least 18 years of age, mentally able and willing to give informed consent
Exclusion Criteria:
- Emergency ablation
- Serious patient condition before ablation
- Physically or mentally unable to provide written informed consent
- Permanent atrial fibrillation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Extended Electrocardiogram
Elective patients receiving an AF ablation receiving a extended ECG
|
ECG with 3 additional leads and a 5 minute recording
|
Body surface potential map
Elective patients receiving an AF ablation receiving a body surface potential map
|
ECG with 184 leads and a 5 minute recording
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Recurrence of AF after ablation
Time Frame: 12 months
|
The predictive value for recurrence of AF in patients after ablation of AF based on atrial conduction characteristics in electrocardiographic, -anatomical, biomarker and genetic analysis
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
AF characteristics
Time Frame: 12 months
|
Identify characteristics of patients with self-terminating in contrast to patients with persistent AF in the registry data
|
12 months
|
ECG AF characteristics
Time Frame: 3 months
|
Identify changes by ablation and convalescence in the extended surface ECG
|
3 months
|
ECG to BSPM discriminative power
Time Frame: 12 months
|
To compare the registry data with a subgroup analysis receiving additional to the routine diagnostics a body surface potential map (BSPM) and an ECG-Imaging (ECGI)
|
12 months
|
Collaborators and Investigators
Collaborators
Investigators
- Study Director: Laurent Pison, Physician, Maastricht University
- Principal Investigator: Ulrich Schotten, Physician, Maastricht University
- Study Director: Matthias D Zink, Physician, Maastricht University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- METC 16-4-208
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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