Multicenter Evaluation of Patients Using LATITUDE Monitoring System
Recruiting · NCT06311149 · Observational (researchers observe without assigning treatment)
View the official record on ClinicalTrials.gov →What this trial is about
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.
Who can take part
Inclusion criteria
- 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 criteria
- 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.
Where it is running
3 locations listed.
- Azienda Ospedaliero-Universitaria di Ferrara - Ferrara, Italy
- Policlinico Federico II - Naples, Italy
- Ospedale "G.B. Grassi" - Roma, Italy