Aortic Aneurysm, Abdominal
Conditions
Keywords
EVAR, AAA, Anchor
Brief summary
Single center, open label, prospective, single-arm, first-in-human (FIH), pre-market clinical study with the objective of validating the safety and performance of the Suture-Tight™ Suture Delivery System in an EVAR procedure.
Detailed description
Single center, study conducted at the Prince of Wales Private Hospital in Randwick, Australia. Up to 6 subjects may be enrolled. 1 to 3 subjects will complete initial enrollment and be followed for 30-days evaluating procedure and device safety. Additional subjects may be enrolled following the safety review to complete the 6-subject study. All subjects will be followed for six (6) months. Subjects meeting all inclusion and exclusion criteria will be consented to receive an elective endovascular aortic aneurysm repair (EVAR) with graft anchoring utilizing the Suture-Tight device. Procedure and device safety and performance will be evaluated at 1- and 6-months by completing CT scans and KUB x-rays. Data may be used to support a pivotal study of the investigational device and future global regulatory submissions.
Interventions
DEVICESuture-Tight Suture Delivery System
Implantation of the Suture-Tight Suture in the deployment of multiple nitinol sutures to provide augmented fixation and sealing between endovascular aortic graft and the native artery.
Sponsors
Prince of Wales Hospital, Sydney
Vesteck, Inc.
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Subjects meeting all inclusion/exclusion criteria and scheduled for an EVAR procedure.
Eligibility
Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Currently scheduled for an elective endovascular repair of an abdominal aortic aneurysm (AAA) by EVAR with CT scan from within last 4 months. Acceptable AAA parameters include: AAA ≥ 5.0 cm in diameter OR AAA ≥ 4.5 cm in diameter with an increase of ≥ 0.5 cm within the past 6-months or ≥ 1.0 cm over the past 12-months * Neck diameter, length and angulation that meets labeling requirements for the endograft used * Successful EVAR graft placement with no evidence of EVAR-associated serious adverse event.
Exclusion criteria
* Mycotic or inflammatory AAA * Prior surgical repair of an AAA * Renal dialysis or significant chronic renal failure * Evidence of recent acute coronary disease, thrombotic disease, or cerebral infarct * Pregnancy
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Serious Adverse Events related to the Suture-Tight Suture Delivery System | 30-days | Recording of all Serious Adverse Event (SAE) related to the Suture-Tight™ Suture Delivery System procedure or device |
| Analysis of the Suture-Tight endoanchor effectiveness | 30-days | 1. Documentation of Procedural success defined as: * Successful delivery of the Suture-Tight™ Delivery Catheter to the site of intended treatment * Successful removal of Suture-Tight™ Delivery Catheter * Absence of evidence of acute endograft migration or dysfunction at the conclusion of the procedure 2. Absence of a Type 1a Endo Leak 3. Absence of a stent graft migration |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| All cause safety events recorded during the study | 6-months | All-cause SAEs recorded during the EVAR procedure through follow-up. |
| Clinical Performance of the Stent Graft following Suture-Tight implant | 6-months | Evaluation of Changes in Stent graft patency, migration or displacement in follow-up as measured by an abdominal CT scan |
| Clinical Performance of the Suture-Tight following implant | 6-months | Evaluation of the Suture-Tight™ Suture migration, displacement, or fracture as measured by an abdominal CT scan and KUB x-rays. |
Countries
Australia
Contacts
Primary ContactJerald L. Cox, PA
Backup ContactLaura Lund, PhD
Outcome results
None listed