Cathbot—a joint venture between Robocath and MicroPort—has enrolled the last patient in its clinical study in China. This is the first step towards obtaining approval from China’s National Medical Products Administration (NMPA) for the commercialisation of R-One, the robotic percutaneous coronary intervention (PCI) platform, in the Chinese market.
The multicentre clinical study began in November 2021 and has enrolled 149 patients over six months. Four centres participated in the trial: 301 Hospital (Beijing, China), Shanxi Cardiovascular Hospital (Shanxi, China), Meizhou Peoples’ Hospital (Meizhou, China), and the People’s Hospital of Xinjiang Uygur Autonomous Region (Ürümqi, China). The last patient was enrolled in May 2022.
“I am deeply impressed by the accuracy and quick learning curve of R-One. Not only can it complete the positioning of the balloon and stent catheter precisely, it also enables manipulation of two guidewires, one of them being parked in a stand-by path, facilitating complex PCI presenting tortuous and/or calcified lesions. This could reduce the risk of intraoperative and post-operative complications, which would benefit both patients and operators,” said Yundai Chen, director of the cardiology department at 301 Hospital.
“The simple and intuitive design of R-One is very convenient for doctors to operate with. We can get started after only short-term training. Additionally, we can complete the intervention whilst being totally protected by sitting in front of the X-Ray-proof console and manipulating the devices using only the joysticks. We look forward to working with R-One on a daily basis to benefit more patients and doctors,” commented Jian An, department of cardiovascular medicine, dean of the Shanxi Cardiovascular Hospital.
“R-One drastically improves our working conditions. First, we can operate while fully protected from radiation; compared to manual interventions where we need to stand for long hours, only a few centimeters from the X-Ray tube, which can induce serious diseases, like cancer, and orthopaedic injuries. Second, it offers a high level of precision which directly benefits the patient,” added Zhixiong Zhong, dean of the Meizhou Peoples’ Hospital.
“During the clinical trial, R-One has been reliable in several consecutive PCI procedures. This technology will benefit doctors and many patients living with cardiovascular diseases all over the country: today, in China, more than one million procedures are performed annually across roughly 2,000 PCI centres,” noted Yining Yang, dean of the People’s Hospital of Xinjiang Uygur Autonomous Region.
“The completion of this clinical trial is a crucial milestone in our development. It is the first PCI robotic multicentre trial completed in China. I am very impressed with the commitment of the Cathbot team and the medical staff. They worked very hard to make it happen on time and to maintain our strategic plans despite the lockdowns. I sincerely thank all of them. Our greatest global ambition is to be able to better treat cardiovascular diseases. R-One will allow the medical staff to work safely while bringing precision to the intervention,” said Philippe Bencteux, president and founder of Robocath and president of Cathbot.
“We look forward to receiving the results of this study, that will undoubtedly confirm the ease of use and intuitiveness of R-One. This clinical trial is the first step towards the commercialisation of R-One in China,” added Lucien Goffart, CEO of Robocath.
“In the field of vascular robotics, the successful completion of this multicentre clinical trial project with R-One is an important milestone for Cathbot. It is of extraordinary significance for promoting more accurate and intelligent interventional medicine. In the future, R-One will be equipped with 5G and AI features, and combined with technologies such as vascular structure imaging and hemodynamic monitoring to achieve more innovative breakthroughs. Our ambition is to provide the best treatment for patients thanks to accurate, intelligent and better integrated robotic solutions,” concluded Chao He, president of MicroPort MedBot.
Source CardiovascularNews
Duc Tin CLinic
Tin tức liên quan
Performance diagnostique de l’interféron gamma dans l’identification de l’origine tuberculeuse des pleurésies exsudatives
A Mixed Phenotype of Airway Wall Thickening and Emphysema Is Associated with Dyspnea and Hospitalization for Chronic Obstructive Pulmonary Disease.
Radiological Approach to Asthma and COPD-The Role of Computed Tomography.
Significant annual cost savings found with UrgoStart in UK and Germany
Thrombolex announces 510(k) clearance of Bashir catheter systems for thromboembolic disorders
Phone: (028) 3981 2678
Mobile: 0903 839 878 - 0909 384 389