Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07019454

Physician Modified Endovascular Grafts for the Treatment of Elective, Symptomatic or Ruptured Juxtarenal Aortic Aneurysms

Led by Baystate Medical Center · Updated on 2025-06-13

15

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patients who are found to have an aneurysm (bulge) in the abdominal aorta, which is the blood vessel in your abdomen (belly) that supplies blood to most of your lower body, including major organs and your legs. As an aneurysm expands, the walls of the aorta become weak and may rupture (break open), causing a major loss of blood with a high risk of serious problems and death. To avoid this risk, doctors repair aneurysms by either open surgery (incision) or endovascular surgery (covered stents to channel the blood flow). Juxtarenal aneurysms (those that come close to the kidney arteries) present a unique challenge as they are more dangerous to repair by open therapy and do not fit the standard approved endovascular devices. The purpose of this study is to assess the effects of the physician-modified endovascular graft (PMEG) by collecting information about the performance of this investigational medical device. The main graft looks like a pair of pants with very short legs. The top of the pants is placed in the aorta. Then, two smaller grafts go from the main graft and to your iliac arteries (the main arteries supplying blood to your abdomen and legs) to form the legs of the pair of pants. Each graft is packed into a small catheter (a long, flexible plastic tube) that is placed into your aorta through the femoral artery in your groin (top of your leg). The grafts are then placed in the correct position in your aorta by releasing them from the catheters. These grafts are investigational because the research physician has changed them to match patient anatomy (body make up) while protecting blood flow to important vessels. Once the grafts are attached inside the aorta, they will support the area of the aorta that is weakened and bulging. Modifications of the graft will include between one and four holes (fenestrations) near the top of the graft. The holes allow the graft to be located above the renal arteries (the blood vessels that supply blood to your kidneys) without blocking the blood flow to them. One or more of the arteries will also be treated with a stent (metal wire tube) to help keep the arteries open and to keep the arteries connected to the holes that are made for the graft. The device is custom modified for patient specific anatomy. The information collected from this study will be used to show how well patients do when treated with the modified graft, both immediately after surgery and over a long period of time. After the procedure, labs, CT imaging with contrast, XRays and ultrasounds will be done to check the graft at intervals 1 month, 6 months, 12 months and yearly for 5 years. These are standard surveillance studies performed on any endovascular aneurysm repair.

CONDITIONS

Official Title

Physician Modified Endovascular Grafts for the Treatment of Elective, Symptomatic or Ruptured Juxtarenal Aortic Aneurysms

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient is 18 years of age or older
  • Male or non-pregnant female with a negative pregnancy test if of childbearing potential
  • Patient or legally authorized representative has signed informed consent
  • Juxtarenal abdominal aortic aneurysm with at least one of: diameter ≥5.5 cm (male) or ≥5.0 cm (female) or twice normal size; growth >0.5 cm in 6 months; saccular aneurysm at high rupture risk; symptomatic aneurysm; ruptured aneurysm
  • Patent iliac or femoral arteries allowing endovascular access
  • Suitable non-aneurysmal proximal aortic neck ≥2 mm below the lowest renal artery
  • Suitable non-aneurysmal distal iliac artery length ≥15 mm preserving at least one hypogastric artery
  • Suitable proximal aortic neck diameter between 20 and 32 mm
  • Suitable distal common iliac diameter between 8 and 20 mm
  • Juxtarenal aortic neck angulation ≤60°
  • Target branch vessel diameter ≥5 mm
  • Willing to comply with all required follow-up exams
Not Eligible

You will not qualify if you...

  • Mycotic aneurysm or active systemic/local infection increasing endovascular infection risk
  • Unstable angina with worsening or new severe symptoms
  • Major unrelated surgery planned within ±30 days of aneurysm repair
  • History of aortopathic connective tissue disease (e.g., Marfan's or Ehlers-Danlos syndrome)
  • Known allergy or intolerance to anticoagulants, contrast media, stainless steel, nitinol, or gold
  • Body habitus preventing X-ray visualization of the aorta
  • Life expectancy less than 1 year
  • Currently participating in another investigational device or drug trial
  • Medical, social, or psychological conditions preventing treatment or follow-up
  • Thrombus or excessive calcification in the aneurysm neck
  • Branch vessel stenosis ≥80%
  • Treatable with FDA-approved EVAR or FEVAR device and can wait for device availability
  • Eligible and willing to enroll in a manufacturer-sponsored or device study at this or another institution

AI-Screening

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Trial Site Locations

Total: 1 location

1

Baystate Medical Center

Springfield, Massachusetts, United States, 01199

Actively Recruiting

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Research Team

E

Erin Daley, MPH, BS

CONTACT

H

Hazel Marecki, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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Physician Modified Endovascular Grafts for the Treatment of Elective, Symptomatic or Ruptured Juxtarenal Aortic Aneurysms | DecenTrialz