PREDICT Registry
Cardiac Surgery | Acute Aortic Dissection | Thoracic Aorta | Intramural HematomaThis registry is for patients who have been diagnosed with an acute aortic dissection/intramural hematoma (also known as a DeBakey I or Stanford type A dissection/intramural hematoma) and have had the Ascyrus Medical Dissection Stent (AMDS) device implanted.
The purpose of this registry is to collect additional information of the AMDS following market approval. If the AMDS device, together with conventional surgery is effective, it is believed that this could lead to a cure of the dissection (tear) in the aorta, reduced hospitalizations, and decreased risk of additional aorta surgeries in the chest compared to conventional surgery alone.
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Participation Requirements
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Sex:
Female, Male -
Eligible Ages:
18 to 80
Participation Criteria
Inclusion Criteria:
Inclusion Criteria:
1) ≥18 and ≤80 years of age (male or female)
2) One of the following diagnosed within 14 days:
- acute DeBakey type I dissection or intramural hematoma based on CT angiography
Exclusion Criteria:
Exclusion Criteria:
1) <18 years of age or >80 years of age (male or female)
2) Unwilling to comply with the follow-up schedule
3) Refusal to give informed consent
There are several medical and anatomical exclusion criteria that need to also be considered. These will be reviewed and discussed with individual potential candidates.
Study Location
University of Alberta
University of AlbertaEdmonton, Alberta
Canada
Contact Study Team
- Study Sponsored By
- University of Alberta
- Participants Required
- More Information
- Study ID:
Pro00087612