Multicenter Evaluation of Patients Using LATITUDE Monitoring System
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorUniversity Hospital of Ferrara
About this trial
The Multitude is a registry of patients who receive commercially available CIEDs that remotely communicate through the LATITUDE monitoring system and transfer data to a central database.
The registry is designed to constitute a shared environment for the collection, management, analysis and reporting of clinical and diagnostic data, adopted by a network of European scientifically-motivated physicians who use rhythm management diagnostic and therapeutic solutions from Boston Scientific in their clinical practice.
The Multitude study will facilitate the sharing of scientific proposals within a large network of researchers, and it will allow researchers to record the experience with medical devices throughout the device and patient lifecycle.
Eligibility criteria
Qualifiers
Subject is willing and capable of providing informed consent to collect/store/process personal health information by the sponsor or such consent is provided by a legally designated representative, if required by local law or regulation.
prospectively scheduled for receiving a device monitored through the LATITUDE monitoring system
retrospectively enrolled after having received a device monitored through the LATITUDE monitoring system
Disqualifiers
Subject foreseen not to be followed at the enrolling center for at least 1 year after having received the device.
Subject is receiving a device that is not approved for commercial use at the time of procedure.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov