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The goal of this registry is to evaluate the semibranch in branched endovascular aortic repair, which is a new tool in endovascular branched aortic repair.
The main question it aims to answer are: * Patency of the semibranch * Feasibility of the technique regarding cannulation and stentgrafting The participants will treated with the custom made semibranch device and enrolled in the registry if they consent. No change in treatment will be made when enrolled.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Muenster University Hospital
Münster, Germany
Start Date
January 12, 2024
Primary Completion Date
December 31, 2026
Completion Date
March 31, 2027
Last Updated
March 26, 2024
100
ESTIMATED participants
Semibranch CMD branched aortic stentgraft
DEVICE
Lead Sponsor
University Hospital Muenster
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07422129