EBR Systems is the lead sponsor of 4 current clinical trials in our USA, Germany, Australia, UK, France, Italy, Netherlands, Denmark and Switzerland registers. 2 are recruiting patients now. The most common phase is Not applicable. The most-studied condition is Heart Failure.
| Study | Phase | Status | Start | Registers |
|---|---|---|---|---|
|
A Feasibility Study Implant of the WiSE® CRT System With an Intracardiac Pacemaker to Achieve Totally Leadless CRT
NCT06561932 · ClinicalTrials.gov ↗ · Heart Failure
|
Not applicable | Recruiting | 2025-12 | Australia |
|
The WiSE®-UP Study (The WiSE System Utilization & Performance Study)
NCT07098858 · ClinicalTrials.gov ↗ · Heart Failure
|
Observational | Recruiting | 2025-11 | USA |
|
Cardiac Resynchronization Therapy in Previously Untreatable and High Risk Upgrade Patients
NCT02922036 · ClinicalTrials.gov ↗ · Heart Failure
|
Not applicable | Active, closed | 2018-01 | UK, USA, Germany, France, Italy, Netherlands, Australia |
|
WiCS-LV Post Market Surveillance Registry
NCT02610673 · ClinicalTrials.gov ↗ · Cardiac Resynchronization Therapy
|
Observational | Active, closed | 2016-02 | Germany, Denmark, Switzerland |
Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.
A trial with sites in more than one country appears in each of those registers.
Sponsors with the most current trials registered for this condition.
EBR Systems is the lead sponsor of 4 current trials on ClinicalTrials.gov in our USA, Germany, Australia, UK, France, Italy, Netherlands, Denmark and Switzerland registers, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.
Yes. 2 of its 4 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.
Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.
This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.