Suture-Tight™ First-in-Human Safety and Performance Study
- Conditions
- Aortic Aneurysm, Abdominal
- Interventions
- Device: Suture-Tight Suture Delivery System
- Registration Number
- NCT05812768
- Lead Sponsor
- Vesteck, Inc.
- 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.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 6
- 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.
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Suture-Tight Suture-Tight Suture Delivery System Subjects meeting all inclusion and exclusion criteria will receive graft anchoring utilizing the Suture-Tight Suture Delivery System.
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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 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.
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
Trial Locations
- Locations (1)
Prince of Wales Private Hospital
🇦🇺Randwick, New South Wales, Australia