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NCT02418611 Clinical Trial

Use of the Zenith® Dissection Endovascular System to Treat Patients With Acute, Complicated Type B Aortic Dissection

Aortic Dissection Clinical Trial

Official title:
Use of the Zenith® Dissection Endovascular System in the Treatment of Patients With Acute, Complicated Type B Aortic Dissection

Clinical Trial Details — Status: No longer available

Administrative data
NCT number NCT02418611
Other study ID # 11-007 EA
Secondary ID
Status No longer available
Phase N/A
First received April 13, 2015
Last updated June 3, 2015

Study information
Verified date June 2015
Source Cook
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Expanded Access

Clinical Trial Summary

The Zenith® Dissection Endovascular System is indicated for the treatment of patients with acute, complicated type B aortic dissection.

Recruitment information / eligibility
Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years and older
Eligibility Exclusion Criteria:

- Less than 18 years of age

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Device:
• Zenith® Dissection Endovascular System
Instead of making a large incision in the chest, the physician makes a small incision near each hip to insert, and guides the study device(s) into place in the aorta.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Cook
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