Registry following heart patients with implanted devices monitored remotely
Collects data from people with heart rhythm devices sent through remote monitoring.
Plain-language title generated from the registry record
Registry title: Multicenter Evaluation of Patients Using LATITUDE Monitoring System
Key facts
- Where
- Ferrara, Naples, and Roma, ItalySee the 3 sites
Where in Italy
- Azienda Ospedaliero Universitaria di FerraraFerrara, ItalyTaking people
- Policlinico Federico IINaples, ItalyTaking people
- Ospedale "G.B. Grassi"Roma, ItalyTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- University Hospital of Ferrara
- Trial code
- NCT06311149
- Record updated
- 12 August 2024
- Original description
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.Read full original descriptionShow less
Multicenter Evaluation of Patients Using LATITUDE Monitoring System: Multitude Study
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.
Inclusion: 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; Subject is:; 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.
Exclusion: 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.