Correlations Between Arrhythmias and Air Pollution in Patients With Pacemaker and ICD (ARIA)
|ClinicalTrials.gov Identifier: NCT01723761|
Recruitment Status : Completed
First Posted : November 8, 2012
Last Update Posted : July 2, 2015
It is a clinical, observational study to evaluate the correlations among arrhythmias, climatic variables and air pollution in patients with pacemaker and implantable defibrillator (ICD), followed by remote monitoring.
Purpose of the Study: The purpose of this study is to test the hypothesis that changes in climatic variables, such as temperature, pressure and humidity, and changes of particulate matter <10µ (PM10), particulate matter <2.5µ (PM2.5), ozone (O3), carbon monoxide (CO), sulfur dioxide (SO2), nitrogen dioxide (NO2), are associated with an increase of supraventricular and ventricular arrhythmias.
Objectives: The aim of this study is to determine whether changes in variables conditions affect the electrical stability of the myocardium in patients with pacemakers and ICDs.
Population: male and female subjects, aged ≥ 18 years, implanted by a dual-chamber pacemaker, ICD or biventricular ICD (ICD-CRT). A total of 500 subjects from 15 cardiology centers of the Veneto region will be included.
|Condition or disease|
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The primary objectives of this study are as follows:
- Determine if the changes of temperature, pressure and humidity, are associated with an increase of atrial and ventricular arrhythmias.
- Determine if the changes of air pollution (gas and particulate), are associated with an increase of atrial and ventricular arrhythmias.
The secondary objectives of the study are:
- Determine if the changes of air pollution (gas and particulate), are associated with significant changes in mean heart rate, rate variability rate and the percentage of paced beats.
- Determine whether changes in temperature, pressure or humidity, are associated with significant changes in mean heart rate, heart rate variability and the percentage of paced beats.
- Determine if the changes of temperature, pressure and humidity, are associated with an increase in mortality or hospitalization for myocardial infarction or congestive heart failure.
- Determine if the changes of air pollution (gas and particulate), are associated with an increase in mortality or hospitalization for myocardial infarction or congestive heart failure.
Study Design This is a prospective, observational study, which compares the occurrence of atrial and ventricular arrhythmias and changes in physiological parameters, with climatic variables and air pollution.
The study will include 500 subjects and will consist of two periods:
Screening: we will collect baseline characteristics of subjects in the clinical examination. The period recruitment will run for 12 months.
Follow-up: After written informed consent will be signed, subjects who meet the criteria for inclusion will be enrolled in the study and followed up for a minimum period of 12 months. The data obtained from the remote monitoring will be evaluated for the daily values provided for the parameters considered in the study.
Periodical visits in pacemaker clinic will be scheduled at the discretion of the referring cardiologist of the center. The arrhythmic events that will occur in this period, detected by means of remote monitoring or through other clinical evaluations will be recorded. Atrial arrythmias: atrial fibrillation or atrial flutter, supraventricular tachycardia.
Ventricular arrhythmias: ventricular tachycardia, ventricular fibrillation, ventricular extrasystoles.
Physiological variables: average heart rate (24 hours and at rest), heart rate variability, the percentage of paced beats.
In addition, any changes in drug therapies and all clinically relevant events, will be recorded.
During the same period data from monitoring stations of ARPAV (Regional Agency for Environmental Prevention and Protection of Veneto Region) will be collected.
Climatic variables: temperature, humidity, atmospheric pressure. Parameters of air pollution: PM10, PM2.5, O3, CO, SO2, NO2. For each patient, the data from the monitoring station ARPAV of the urban area of residence of the subject will be considered. The mean exposure level used in the analytical studies on the health effects is calculated on the average number of units active in the area. This number is usually of 2-3 units in large centers, while it is generally only 1 in small towns. The residents in centers without monitoring will be excluded from the study. The mean value is the best approximation ... to be continued page 6.
|Study Type :||Observational|
|Actual Enrollment :||473 participants|
|Official Title:||Correlations Between Arrhythmias, Climatic Variables and Air Pollution in Patients With Pacemaker and ICD, Followed by Remote Monitoring.|
|Study Start Date :||April 2011|
|Actual Primary Completion Date :||November 2013|
|Actual Study Completion Date :||June 2015|
- incidence of atrial arrhythmias. [ Time Frame: 12- 24 months. ]The arrhythmic events that will occur during follow-up period, detected by remote monitoring or through other clinical evaluations, will be recorded and classified as follows: atrial fibrillation or atrial flutter, supraventricular tachycardia.
- incidence of ventricular arrhythmias [ Time Frame: 12-24 months ]The arrhythmic events that will occur during follow-up period, detected by remote monitoring or through other clinical evaluations, will be recorded and classified as follows: ventricular tachycardia, ventricular fibrillation, premature ventricular beats.
- Mean heart rate [ Time Frame: 12-24 months ]Mean heart rate obtained by remote monitoring of pacemaker and ICDs.
- Heart rate variability [ Time Frame: 12-24 months ]Measures of heart rate variability calculated by devices and obtained by remote monitoring.
- Percentage of paced beats [ Time Frame: 12-24 months ]Percentage of paced beats will be measured by devices diagnostic and obtained via remote monitoring.
- Mortality for myocardial infarction or heart failure. [ Time Frame: 12-24 months ]
- Hospitalization for myocardial infarction or heart failure. [ Time Frame: 12-24 months ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01723761
|Ospedale S.Maria dei Battuti - Cardiologia|
|Conegliano, Italy, 31015|
|Ospedale di ESte|
|Este, Italy, 35042|
|Legnago, Italy, 37045|
|Mestre, Italy, 30175|
|Mirano, Italy, 30039|
|Ospedale S. Valentino|
|Montebelluna, Italy, 31044|
|Dipartimento di Scienze Cardiologiche, Toraciche e Vascolari-Università di Padova|
|Padova, Italy, 35128|
|Portogruaro, Italy, 30026|
|Ospedale Ca' Foncello - Divisione di Cardiologia|
|Treviso, Italy, 31100|
|Principal Investigator:||Gianfranco Buja, MD||University of Padua|