Study of the RelayPro Thoracic Stent-Graft in Subjects With an Acute, Complicated Type B Aortic Dissection

This clinical trial is a prospective, multicenter, non-blinded, non-randomized study designed
to assess the RelayPro thoracic endografts in the treatment of acute, complicated type B
aortic dissection. The primary endpoint will measure all-cause mortality at 30 days
post-procedure.

Subjects will be enrolled on a first come, first serve basis; however, no single
investigational site may enroll more than 20% of the proposed sample size of up to 80
subjects. A subject is considered enrolled when arterial access is gained and an attempt is
made to introduce the RelayPro Thoracic Stent-Graft. Enrollment is expected to begin in
mid-2016 and complete by the end of 2020.

All subjects enrolled, as defined above, will be included in the patient population for the
primary safety analyses. All subjects implanted with the RelayPro Thoracic Stent-Graft will
be included in the patient population for the primary effectiveness analyses.

Inclusion Criteria:

- Subject must have an acute (symptom onset to diagnosis within 2 weeks)or subacute,
complicated type B aortic dissection (entire dissection is distal to the left
subclavian artery (LSA)), confirmed by Computed Tomography Angiography (CTA) or
Magnetic Resonance Angiogram (MRA), with time from symptom onset to diagnosis ≤ 6
weeks, with at least one of the following:

- Malperfusion of the viscera, kidneys, spinal cord, or lower extremities, measured
by clinical or radiographic evidence;

- Rupture;

- Intractable pain.

- Proximal and distal aortic neck with diameter between 19 mm and 42 mm.

- Subject's anatomy must meet all of the following anatomical criteria:

1. Proximal attachment zone distal to the left common carotid and a distal
attachment zone proximal to the origin of the celiac artery. (Dissection is
permitted in the distal attachment zone but is not permitted in the proximal
attachment zone.)

2. The length of the attachment zones will depend on the intended stent-graft
diameter and type of graft selected.

3. The proximal attachment zone should be 15 mm for 22 - 28 mm RelayPro grafts with
bare stent (20 mm for RelayPro grafts with non-bare stent), 20 mm for 30 - 46 mm
RelayPro grafts with bare stent (25 mm for RelayPro grafts with non-bare stent),
and proximal to non-dissected segment (healthy zone).

4. The distal attachment zone should be 20 mm for all RelayPro grafts.

5. Coverage of the left subclavian artery is permitted with mandatory
revascularization if patent left internal mammary artery (LIMA) bypass or left
upper extremity (LUE) arteriovenous graft or anomalous vertebral artery off the
aorta. Revascularization must be performed prior to device placement, and may
occur during implant procedure, provided it is before coverage of the LSA by the
endograft.

- Proximal attachment zone containing a straight segment (non-tapered,
non-reverse-tapered, defined by <10% diameter change) with lengths equal to or greater
than the required attachment length for the intended device.

- Vascular dimensions (e.g., aortic diameters, length from left subclavian to celiac
artery) must be in the range that can be safely treated with the RelayPro Thoracic
Stent-Grafts.

- Adequate iliac or femoral artery access for introduction of the RelayPro Delivery
System. Alternative methods to gain proper access may be utilized (e.g., iliac
conduit).

- Subject willing to comply with the follow-up evaluation schedule.

- Subject (or Legally Authorized Representative, LAR) agrees to sign an Informed Consent
Form prior to treatment.

Exclusion Criteria:

- Diagnosis of traumatic injury or transection of the descending thoracic aorta.

- Significant stenosis, calcification, thrombus, or tortuosity of intended fixation
sites that would compromise fixation or seal of the device.

- Planned coverage of left carotid or celiac arteries; or anatomic variants that would
compromise circulation to the carotid, vertebral, or innominate arteries after device
placement, which is not amenable to subclavian revascularization.

- Prior endovascular or surgical repair in the descending thoracic aorta. The device may
not be placed within any prior endovascular or surgical graft.

- Concomitant aneurysm/disease of the ascending aorta, aortic arch, or abdominal aorta,
requiring repair. Dissection extension into the abdominal aorta is acceptable.

- Prior abdominal aortic aneurysm repair (endovascular or surgical) that was performed
less than 6 months prior to the planned stent implant procedure.

- Major surgical or medical procedure within 30 days prior to the planned procedure, or
is scheduled for a major surgical or medical procedure within 30 days post
implantation. This excludes any planned procedures for the prospective stent-graft
placement.

- Untreatable allergy or sensitivity to contrast media or device components, including
metal stents.

- Known or suspected connective tissue disorder.

- Blood coagulation disorder or bleeding diathesis for which the treatment cannot be
suspended for one week pre- and/or post-repair.

- Coronary artery disease with unstable angina.

- Severe congestive heart failure (New York Heart Association functional class IV).

- Stroke and/or Myocardial Infarction (MI) within 3 months of the planned treatment
date.

- Pulmonary disease requiring the routine (daily or nightly) need for oxygen therapy
outside the hospital setting.

- Acute renal failure or chronic renal insufficiency, and not receiving dialysis.

- Hemodynamically unstable.

- Active systemic infection and/or mycotic aneurysms.

- Bowel necrosis.

- Morbid obesity or other condition that may compromise or prevent the necessary imaging
requirements.

- ASA risk classification = V (Moribund patient not expected to live 24 hours with or
without operation).

- Less than two-year life expectancy.

- Current or planned participation in an investigational drug or device study that has
not completed primary endpoint evaluation.

- Currently pregnant or planning to become pregnant during the course of the study.

- Medical, social, or psychological issues that Investigator believes may interfere with
treatment or follow-up.