NCT06311149Recruiting
Multicenter Evaluation of Patients Using LATITUDE Monitoring System
Multicenter Evaluation of Patients Using LATITUDE Monitoring System: Multitude Study
Source: ClinicalTrials.gov · Last updated 12 Aug 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 20000 (estimated)
- First submitted
- 7 Mar 2024
- Start date
- 1 Dec 2023
- Primary completion date
- 31 Dec 2043
- Lead sponsor
- University Hospital of Ferrara
- Diseases
- Heart failure
- NCT number
- NCT06311149
What you commit to
- Study type: Observational
- Planned participants: 20000
- From 1 Dec 2023 to the primary completion date, 31 Dec 2043
- 3 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- 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.
Who the study is looking for
- 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
Sex: All · Does not accept healthy volunteers
Sites (3)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Azienda Ospedaliero Universitaria di Ferrara Coordinator of this site? Confirm its status | Ferrara | Italy | Recruiting |
| Policlinico Federico II Coordinator of this site? Confirm its status | Naples | Italy | Recruiting |
| Ospedale "G.B. Grassi" Coordinator of this site? Confirm its status | Roma | Italy | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.