Suture-Tight™ First-in-Human Safety and Performance Study

Vesteck

Status: Enrolling

Conditions: Aortic Aneurysm, Abdominal

Treatments: Device: Suture-Tight Suture Delivery System

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05812768

CLP-05

Details and patient eligibility

About

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.

Full 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.

Enrollment: 6 estimated patients

Sex: All

Ages: 21 to 80 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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6 participants in 1 patient group

Suture-Tight

Experimental group

Description:

Subjects meeting all inclusion and exclusion criteria will receive graft anchoring utilizing the Suture-Tight Suture Delivery System.

Treatment:

Device: Suture-Tight Suture Delivery System