Full Early Atrial Diagnostics in Single Chamber ICD Patients Using the DX Lead and Home Monitoring in Brazil.
- Conditions
- Arrhythmias, Cardiac
- Registration Number
- NCT04869527
- Lead Sponsor
- Biotronik SE & Co. KG
- Brief Summary
To demonstrate the value and benefits of BIOTRONIK's exclusive DX technology in assessing the incidence of supraventricular arrhythmias, mainly atrial fibrillation (AF), in patients with an indication for single chamber ICDs.
Effects of the DX technology on related events, such as delivery of therapies and medical management, including eventual complications.
Extended benefits offered by DX devices when associated with daily remote monitoring, by means of BIOTRONIK's Home Monitoring Service Center (HMSC).
- Detailed Description
To demonstrate the value and benefits of BIOTRONIK's exclusive DX technology in assessing the incidence of supraventricular arrhythmias, mainly atrial fibrillation (AF), in patients with an indication for single chamber ICDs.
Effects of the DX technology on related events, such as delivery of therapies and medical management, including eventual complications.
Extended benefits offered by DX devices when associated with daily remote monitoring, by means of BIOTRONIK's Home Monitoring Service Center (HMSC).
Primary Endpoint:
- First confirmed episode of AF or atrial flutter (AFL) or supraventricular tachycardia (SVT), detected and transmitted to the HMSC.
Other events of interest:
* Rate of successful transmissions received and stored on the HMSC platform;
* Hospital admissions related to cardiologic outcomes, at any time throughout the FU period;
* A composite outcome of any of the following device-related complications: Need for any lead repositioning or replacement, pneumothorax, new pericardial effusion, tamponade, procedure-related death or wound infection, within 60 days after the ICD insertion.
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 50
- Indication for implanting of a single chamber ICD (primary or secondary prevention) according to current guidelines;
- Sustained sinus rhythm as the current prevalent atrial rhythm;
- Planned de novo implantation with a BIOTRONIK single chamber DX ICD system;
- Patient is able to understand the nature of study and to provide written informed consent;
- Patient is willing and able to perform all follow up visits at the study site;
- Patient is willing and able to use the CardioMessenger and accepts the BIOTRONIK Home Monitoring concept.
- Age < 18 years
- Any limitation to contractual capability;
- Female patients who are pregnant or breast feeding or planning pregnancy during the course of the study;
- Known active malignant disease or recovered from malignant disease within 2 years prior to enrollment;
- Life expectancy < 2 years;
- Patient is participating in any other interventional clinical investigation.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Atrial Flutter or Supraventricular Tachycardia 12 months First confirmed episode of AF or atrial flutter (AFL) or supraventricular tachycardia (SVT), detected and transmitted to the HMSC.
- Secondary Outcome Measures
Name Time Method Cardiologic hospitalization 12 months Number of participants with hospital admissions related to cardiologic outcomes, at any time throughout the FU period;
Device related complication 60 days A composite outcome of any of the following device-related complications: Number of patients who need for any lead repositioning or replacement, pneumothorax, new pericardial effusion, tamponade, procedure-related death, or wound infection, within 60 days after the ICD insertion.
Successful transmission HMSC platform 12 months Number of participants with successful transmissions received and stored on the HMSC platform
Trial Locations
- Locations (2)
Santa Casa de Misericórdia de Porto Alegre - Brugada Institute
🇧🇷Porto Alegre, Rio Grande Do Sul, Brazil
BIOTRONIK Coml Médica LTDA
🇧🇷São Paulo, Brazil