Columbia, MONCT06411990Now EnrollingIRB Ready

Aortic Aneurysm Clinical Trial in Columbia, MO

Access cutting-edge aortic aneurysm treatment through this clinical trial at a research site in Columbia. Study-provided care at no cost to qualified participants.

Sponsored by Jonathan Bath

Quick Self-Assessment

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Expert Care in Columbia

Access aortic aneurysm specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related aortic aneurysm treatment provided free

Apply for This Columbia Location

Check if you qualify for this aortic aneurysm clinical trial in Columbia, MO

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Columbia

    Convenient for MO residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Columbia site if eligible
  4. 4Begin participation

About This Aortic Aneurysm Study in Columbia

The goal of this clinical trial is to learn about a new device, named the LIFE device, to treat people with aneurysms (swellings) in the aorta (large, main blood vessel that delivers blood from the heart to the body). The main questions this trial aims to answer are: * If the LIFE device works to treat aortic aneurysms * What medical problems participants have when the LIFE device is used Participants will undergo treatment with the LIFE device and thereafter at 30 days, 6 months, 1 year, 2 years, 3 years, 4 years, and 5 years have their pulses checked, bloodwork to check kidney function (BUN and serum creatinine), and a CT scan of the aneurysm area.

Sponsor: Jonathan Bath

Who Can Participate

Inclusion Criteria

Aortic aneurysm \>5.5 cm in a man or \> 5.0 cm in a woman or rapid expansion deemed at significant risk for rupture in the juxtarenal or pararenal aorta.
Endovascular aortic repair requiring coverage of renovisceral branches.
Not candidate or at high risk for open repair. For example, but not exclusively, due to renal dysfunction, previous abdominal surgery, obese body habitus, previous coronary bypass grafts or high cardiac risk, chronic obstructive pulmonary disease (COPD) or on oxygen at rest, poorly controlled diabetes, current smoking, or antiplatelet or anticoagulation use.
Proximal aortic landing zone in Zone 5 of the aorta or previous graft of at least 10 mm in length and diameter of between 20 and 40 mm.
Distance ≥ 5 mm between top of graft fabric and renovisceral branch orifice.
At least a 5 mm iliofemoral artery to accept the endovascular stent graft device and an axillary brachial artery of sufficient diameter to accept the laser catheter.
Renovisceral diameter between 4 and 13 mm at the origin.
At the time of case planning, the patient's anatomy appears amenable to complete

Exclusion Criteria

of the aneurysm with laser fenestration techniques.
Not willing or able to travel to sites that have access to manufacturer-made investigational endovascular devices.
Not a candidate for currently approved endovascular options.
18 years or older.
Patient or legally authorized representative agrees to participate in the study and provides written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization.
Patient is able and willing to meet all study requirements, including participating in follow up evaluations and attending required assessment visits. Exclusion Criteria:
Known sensitivities or allergies to the materials of construction of the devices, including Nitinol, polyester, Platinum-Iridium, stainless steel, fluoropolymer, and heparin.
Known hypersensitivity or contraindication to anticoagulation or contrast media that cannot be adequately medically managed.
Uncorrectable coagulopathy.
Body habitus that would inhibit radiographic visualization of the aorta or exceeds the safe capacity of equipment.
Concurrent participation in another research protocol for investigation of an experimental therapy.
Subject has been judged to be unsuitable for participation in the study by the Investigator for any reason.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Columbia?

Yes, this clinical trial (NCT06411990) has an active research site in Columbia, MO that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Aortic Aneurysm Treatment Options in Columbia, MO

If you're searching for aortic aneurysm treatment options in Columbia, MO, this clinical trial (NCT06411990) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Columbia research site is actively enrolling participants for this clinical trial. You'll receive care from experienced aortic aneurysm specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all aortic aneurysm clinical trials near you to find additional studies recruiting in your area.

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