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Clinical Trial Summary

The study results will be used to check the hypothesis that CareLink Express remote monitoring system increases the detection rate of asymptomatic AF and allows to change timely the treatment strategy in patients at high risk of thromboembolic events, e.g. anticoagulation therapy onset, electrical cardioversion or/and PVI.


Clinical Trial Description

It is expected to enroll 200 consecutive patients without previously diagnosed AF, who have indications for implantation of dual chamber cardiac pacemakers according to the current guidelines. All the patients will be randomly assigned into 2 groups. Patients in the RM group will undergo the implantation of Ensura DR MRI SureScan pacing system, whereas patients in the control group will receive ADAPTA DR pacing system without RM using. The impact of the Care Link Express service on prevention of thromboembolism will be evaluated. The rate of in-hospital visits for 1 patient per year and compliance with scheduled CareLink transmissions (ratio of the number of the performed transmissions to the planned ones) will be assessed in all patients in the remote monitoring group. Moreover, we are going to estimate the interaction between the follow-up center and other healthcare facilities equipped with the CareLink Express service, which will facilitate faster treatment decision. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04306978
Study type Interventional
Source Research Institute for Complex Problems of Cardiovascular Diseases, Russia
Contact Sergey E Mamchur, M.D., Ph.D.
Phone +79132985516
Email sergei_mamchur@mail.ru
Status Recruiting
Phase N/A
Start date September 21, 2017
Completion date January 21, 2023

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