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New treatment option for Aortic Aneurysm
Official title Laser In Situ Fenestration Study
ClinicalTrials.gov ID: NCT06411990
What this study is testing
- What it's testing
- 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.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- 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...
- 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...
- 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.
You likely can't join if
- Known sensitivities or allergies to the materials of construction of the devices, including Nitinol, polyester, Platinum-Iridium, stainless steel...
- 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.
See the full eligibility 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...
- 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 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.
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Columbia, Missouri, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Columbia, Missouri, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.