Nectero EAST System Retreatment Study

Trial details

Who runs it

Nectero Medical, Inc.

Trial code

NCT07505082

Record updated

26 May 2026

Original description

This is an exploratory pilot study to evaluate the safety and clinical utility of retreatment with an investigational combination product called the Nectero EAST System to treat Abdominal Aortic Aneurysms or AAA.Read full original descriptionShow less

A Clinical Pilot Study to Evaluate the Safety and Clinical Utility of Retreatment With the Nectero EAST System for Stabilization of Abdominal Aortic Aneurysms

This is an exploratory pilot study to evaluate the safety and clinical utility of retreatment with an investigational combination product called the Nectero EAST System to treat Abdominal Aortic Aneurysms or AAA.

Inclusion: Received initial Nectero EAST System treatment under protocol CTP-001; Males and females ≥21 to ≤85 years of age. Females must be of non-childbearing potential (menopause or sterilization); Subject understands the purpose of the trial, agrees to voluntarily participate in the trial, signs the informed consent and is willing to complete the follow-up according to the requirements of the protocol; Infrarenal atherosclerotic fusiform abdominal aortic aneurysm ≤5.3 cm (male) and ≤4.8 cm (female); Infrarenal aortic neck ≥ 15 mm in length and ≤ 29 mm in diameter; Overall AAA treatment length (distal renal artery to distal inferior margin of the aneurysm) not to exceed 130 mm; Iliac and femoral artery access, vessel size and morphology allow endovascular access of 14F (or larger) introducer sheaths and catheters; Subject meets American Society of Anesthesiology (ASA) grade 1 through 3 criteria, inclusive; Subject has > two-year life expectancy; Subject is able and willing to comply with all required follow-up clinic visits including CT scans (screening, 6, 12, 24 months) and blood draws.

Exclusion: Previous surgical or endovascular aneurysm repair for abdominal aortic aneurysm; Subject has had a myocardial infarction within six (6) months prior to enrollment or elevated CK enzymes or troponin indicative of an evolving MI prior to procedure; Subject has undergone other major surgery within the 30 days prior to enrollment; Known contraindication to undergoing angiography or receiving systemic anticoagulation during the procedure; Subject is participating in another research trial that could interfere with the results of the trial (e.g., drug trial); Subjects with rapidly expanding AAA (previous diameter increases of ≥0.5 cm in 6-months or ≥1 cm in 1 year) as these should be evaluated for immediate repair; Subject has a mycotic or infected aneurysm; Subject has current angina, unstable angina, or other active cardiac condition such as congestive heart failure III and IV, atrial arrhythmia, ventricular arrhythmia, or valvular disease, requiring intervention; Subjects with any transient ischemic attack (TIA) or ischemic stroke within 3 months; Known allergy to contrast material that cannot be adequately premedicated, delivery system materials (i.e., nylon, polyurethane) and/or pentagalloylglucose (PGG); Subject is morbidly obese or has other clinical conditions that severely inhibit X-ray visualization of the aorta; Subject has connective tissue/collagen disorder (e.g., Marfan syndrome, vascular Ehlers-Danlos Syndrome, Loeys-Dietz Syndrome, Eaton Syndrome, Bessel-Hagen disease, etc.); Subject has active systemic infection; Subjects with active/acute or a history of unstable chronic liver disease or current liver disease including but not limited to liver transplant, known genetic disorders such as Gilbert syndrome or other liver diseases; Subjects with uncontrolled alcohol use disorder or current alcohol use putting them at risk of liver disease: including consumption of above one standard drink per day for women and two standard drinks per day for men; Subjects with known right-sided heart failure or pathologically dilated inferior vena cava or hepatic veins indicative of congestive hepatopathy; Subject has dialysis dependent renal failure or baseline serum creatinine level >2.5mg/dL or eGFR < 45 mL/min/1.73m2; Subjects with aminotransferase (ALT and/or AST) which is ≥1.5x upper limit of normal (ULN) or TB is out of normal range for the evaluating laboratory; Subjects with INR out of normal range for the evaluating laboratory for a subject not on anti-coagulant therapy; or INR >3 for a subject on anti-coagulant therapy; Subject has an acutely ruptured, leaking, dissecting or emergent aneurysm; Subject has a symptomatic infrarenal abdominal aortic aneurysm; Subject has current vascular injury due to trauma; Subject's aneurysm is thoracic, suprarenal or juxtarenal; Subject has anatomy of diffuse, ulcerated, or extensive (shaggy) thrombus in the neck of the AAA, that in the opinion of the vascular surgeon/investigator, could result in embolization of the thrombus; Subject has anatomy of calcification, and/or plaque within the ilio-femoral arteries or severe infrarenal neck angulation that may compromise or does not allow delivery of the Introducer Sheath or the delivery catheter of the Nectero EAST System; Subject has other medical, social, or psychological problems that, in the opinion of the investigator, preclude them from participation in the trial and to undergo the procedures and evaluations pre- and post-treatment; Subjects that may not tolerate the lowering of their systolic blood pressure to approximately 100mmHg, should not be considered for this study or treated using the Nectero EAST System; Subjects that may not be able to tolerate transient occlusion of the aorta should not be considered for this study; Subjects with saccular AAA; Subjects who are not suitable for the Nectero EAST System treatment, as determined by the investigator; Subjects with cirrhosis (e.g., known history or new clinical diagnosis by elastography with a fibrosis score of F3 or F4 and/or steatosis grade of S3).

ClinicalTrials.gov NCT07505082