CONventional Antegrade vs Sub-Intimal Synergy sTENTing in Chronic Total Occlusions
Status: Unknown
Location: See all (6) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The purpose of this study is to demonstrate that enhanced vascular healing with the Synergy stent should minimize the risk of late aneurysm formation and potential clinical complications but not at the cost of enhanced efficacy.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Male or female patient \>18 years old
• Females of childbearing potential with a negative pregnancy test
• Presence of Chronic Total Occlusion (CTO) that is known or presumed to be of at least 3 months in duration
• Subject (or legal guardian) understands the trial requirements and the treatment procedures and provides written informed consent
• Attempt to implant at least one Synergy II stent has been made
Locations
Other Locations
United Kingdom
Belfast Health & Social Care Trust
Belfast
Bristol Royal Infirmary
Bristol
Edinburgh Royal Infirmary
Edinburgh
Golden Jubilee, Glasgow
Glasgow
Kings College, London
London
London Chest Hospital,
London
Time Frame
Start Date: 2014-12
Completion Date: 2018-12
Participants
Target number of participants: 215
Treatments
Patient with chronic total occlusion
Authors
Related Therapeutic Areas
Sponsors
Collaborators: Ceric Sàrl
Leads: European Cardiovascular Research Center