Descending Aortic Dissection
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Uncomplicated Type B Dissection in the past 2 weeksAged 18 years or older at the time of informed consent signature
Exclusion criteria
Exclusion criteria: Participants with no signed informed consentScheduled surgical or endovascular treatment of Type B DissectionParticipants previously treated in their descending aorta, either open surgery or TEVARSeverely impaired renal function (eGFR < 30mL/min/1.74m2)Participants with traumatic aortic dissectionsParticipants with an established connective tissue disease, including but not limited to Marfans and Loeys-Dietz syndromePregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Composite outcome of positive false lumen development: full thrombosis of the false lumen, or no false lumen diameter growth over 3-mm per year during one year follow-up. | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of Life and physical and mental health status during 1-year follow-upPercentage of thrombosed false lumen during 1-year follow-upChange in volume of the false lumen during 1-year follow-upChange in maximal descending aortic diameter during 1-year follow-upChange in descending aortic volume during 1-year follow-upAortic-related mortality, hospital readmission, organ malperfusion, TEVAR | — |
Countries
Netherlands
Contacts
Rijnstate