Change History and Adopt a Robotic SolutioN for anGioplasty procedurE
Condition(s) studied
Investigational drug(s) / intervention(s)
Robotic-assisted PCI: Robotic-assisted PCI will be performed according to the routine hospital practices, current scientific guidelines and following Instructions for Use (IFU) provided by the manufacturer
Study summary
The main objective of the CHANGE registry is the evaluation of the real-world performance and safety profile of the R-One System in PCI.
Eligibility
Primary outcome measure(s)
- Clinical success — From Day 0 to Day 3
Less than 30% residual stenosis (visual estimate) post PCI in the lesion(s) treated with the R-One System, without in-hospital major adverse cardiac events (MACE). - Technical success — During procedure
Absence of any unplanned manual assistance or conversion to manual PCI for procedural completion
Trial sites (8)
| Facility | City | Region | Status |
|---|---|---|---|
| Het Ziekenhuisnetwerk Antwerpen vzw | Antwerp | Belgium | Recruiting |
| Brest university hospital | Brest | Brittany Region | Recruiting |
| Rouen university hospital | Rouen | France | Recruiting |
| Centre Cardiologique du Nord | Saint-Denis | Île-de-France Region | Recruiting |
| Rheinland Klinikum Neuss GmbH | Neuss | Lukaskrankenhaus | Recruiting |
| San Donato Policlinco Kardia | San Donato Milanese | MI | Not Yet Recruiting |
| Polskie Towarzystwo Kardiologiczne | Warsaw | Par Défaut | Not Yet Recruiting |
| Netcare Christiaan Barnard Memorial Hospital | Cape Town | le Cap | Not Yet Recruiting |
More Robocath trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05853419 on ClinicalTrials.gov ↗ ← All trials in France