Physician-Sponsored IDE for Talent Endoluminal Spring Graft System in Patients With Abdominal Aortic Aneurysms (AAA)

NCT ID: NCT00695253

Last Updated: 2023-02-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 49 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-04-30
• Study Completion Date: 2013-03-31

Brief Summary

The purpose of this study is to evaluate the safety and effectiveness of the Talent Endoluminal Spring Graft System, an investigational device, to treat abdominal aortic aneurysms (AAA). The treatment population will include patients with an abdominal aortic aneurysm who meet the inclusion/exclusion criteria. All patients in the treatment population will undergo post-procedure follow-up evaluations at one (1), six (6), and 12 months and annually thereafter up to five (5) years post-procedure.

Detailed Description

Endovascular aneurysm repair (EVAR) offers certain advantages as compared to surgical repair of an abdominal aortic aneurysm. Known benefits associated with EVAR, as described in scientific literature, include minimally invasive procedure, shorter ICU and hospital stay, reduced blood loss, more rapid recovery, and reduced need for general anesthesia. Potential benefits that may be associated with use of the Talent device include reduced occurrence of endoleaks, therefore reduced subsequent re-interventions. The risks/complications known to occur to all patients undergoing AAA repair may include anesthetic complications, (e.g., aspiration), aneurysm enlargement, rupture, perforation or dissection, bleeding, arterial or venous thrombosis and/or pseudoaneurysm, arteriovenous fistula, hematoma or coagulopathy, bowel complications, cardiac complications, (e.g., arrhythmia, myocardial infarction, congestive heart failure, hypotension, hypertension), embolization (micro and macro) with transient or permanent ischemia or infarction, genitourinary complications, infection, neurologic complications, occlusion of device or native vessel, pulmonary/respiratory complications and renal complications.

Conditions

Abdominal Aortic Aneurysms

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Talent Endoluminal Spring Graft System

Single Arm study of the endoluminal treatment of Abdominal Aortic Aneurysms using the Talent Endoluminal Spring Graft System

Group Type: OTHER

Talent Endoluminal Spring Graft System

Intervention Type: DEVICE

Endovascular repair for patients with AAA who meet the inclusion criteria for the study

Interventions

Talent Endoluminal Spring Graft System

Endovascular repair for patients with AAA who meet the inclusion criteria for the study

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Subjects who participate in this study must fulfill all of the following criteria.
• Subject is > 18 years of age.
• Subject is not pregnant, and, if female and of child-bearing potential, is practicing contraception.
• Subject has documented evidence of at least one patent internal iliac artery.
• Subject has an AAA that is dilated to > 4 cm in diameter.
• Subject has a proximal AAA neck (distance between the top of the aneurysm and the renal arteries) > 5 mm.
• Subject has a proximal aortic neck diameter > 14 mm and < 32 mm.
• Subject has an angle between the suprarenal aorta and the aneurysm <60o.
• Subject has renal arteries > 9 cm from the aortic bifurcation.
• Subject has proximal and distal iliac neck diameters > 8 mm and < 18 mm to accommodate stock devices. For those subjects whose proximal and distal iliac diameters are > 18 mm, custom devices with a variation in fixation diameters will be ordered from the manufacturer.
• Subject has a distal iliac neck length > 15 mm.
• Subject has signed informed consent.
• Subject will be available for follow-up for 12 months after the procedure.

Exclusion Criteria

• Subjects who fulfill any of the following criteria may not participate in this study.
• Subject has patent internal iliac arteries that require graft extension to the external iliac arteries.
• Subject has one or more patent subrenal arteries with potential retrograde flow after stent-grafting.
• Subject has a dominant patent inferior mesenteric artery and an occluded or stenotic celiac and superior mesenteric artery.
• Subject has an aneurysm involving both internal iliac arteries.
• Subject has a lesion that cannot be crossed with a guide wire.
• Subject whose arterial access site cannot accommodate the delivery catheter.
• Subject has no distal vascular bed.
• Subject has systemic infection, or is suspected of having systemic infection.
• Subject has contraindications for use of contrast medium or anticoagulation drugs.
• Subject has received a previous stent in the subrenal aorta.
• Subject has an untreatable bleeding diathesis.
• Subject is in a hypercoagulable state.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Rodney A. White, M.D.

OTHER

Sponsor Role: lead

Responsible Party

Rodney A. White, M.D.

Chief, Vascular Surgery

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Rodney A. White, M.D.

Role: PRINCIPAL_INVESTIGATOR

Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center

Locations

LAC Harbor-UCLA Medical Center

Torrance, California, United States

Countries

United States

Other Identifiers

10807-01

Identifier Type: -

Identifier Source: org_study_id