Zenith® TXD Post-market Surveillance in Japan

Cook Group

Status: Completed

Conditions: Aortic Dissection

Treatments: Device: Zenith® TXD

Study type: Observational

Funder types: Industry

Identifiers

NCT02663739

13-12

Details and patient eligibility

About

The study is a post-market surveillance study required by Japanese Regulatory Authorities as a condition of approval

Enrollment: 57 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients with thoracic aortic dissection, including attempted cases
• Patients with acute Stanford type B aortic dissection, including attempted cases

Exclusion criteria

• Stanford type A aortic dissection and/or chronic type B aortic dissection

Trial design

57 participants in 1 patient group

Aortic Dissection

Description:

Treating patients with acute complicated Stanford Type B aortic dissection with the Zenith® TXD

Treatment:

Device: Zenith® TXD