Status:
COMPLETED
The NEXUS™ Compassionate Use Data Collection Study
Lead Sponsor:
Endospan Ltd.
Conditions:
Aortic Arch Aneurysm
Eligibility:
All Genders
Brief Summary
A Multicenter, observational Data Collection Study to Evaluate the Safety and Performance of the Nexus™ Aortic Arch Stent Graft System in patients that were implanted with the device as part of Compas...
Detailed Description
The purpose of the study is to collect and analyze data that is recorded as standard of care for patients that were implanted with the Nexus device as part of Compassionate Use Procedures.The data wil...
Eligibility Criteria
Inclusion
- Patients for whom the Nexus implantation was initiated as part of a compassionate use procedure.
- A signed and dated Informed Consent document is available that authorizes to collect the patient's personal data following implantation of the Nexus systems and throughout the follow ups visits up to 5 years following implantation.
Exclusion
- There are no exclusions. Data will be collected for all implanted population as described in the inclusion section above
Key Trial Info
Start Date :
February 19 2018
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
November 28 2023
Estimated Enrollment :
7 Patients enrolled
Trial Details
Trial ID
NCT03420066
Start Date
February 19 2018
End Date
November 28 2023
Last Update
January 5 2024
Active Locations (4)
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1
Ospedale San Filippo Neri
Rome, Lazio, Italy, 00135
2
ADHB Charitable Trust
Auckland, New Zealand
3
Klinik Hirslanden
Zurich, Switzerland, CH-8032
4
Zurich University Hospital
Zurich, Switzerland, CH-8091