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RECRUITING NA

Laser In Situ Fenestration Study

NCT06411990 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DEVICE Fenestrated Endovascular Aneurysm Repair using the LIFE Device System

Study Locations (1)

Missouri

  • University of Missouri - Columbia — Columbia

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2024-10-15
Est. Completion 2031-06
Phase NA

Sponsor

Jonathan Bath

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06411990

The ClinicalTrials.gov registry entry for NCT06411990 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Jonathan Bath, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Aortic Aneurysm appearing as the primary indexed condition, and to 1 intervention — of which Fenestrated Endovascular Aneurysm Repair using the LIFE Device System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06411990 reports 1 study location spanning 1 distinct geographic area — top geographies include Missouri. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06411990 about?

NCT06411990 is a clinical study titled "Laser In Situ Fenestration Study". 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 t...

What is the current status of trial NCT06411990?

This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2024-10-15. Estimated completion is 2031-06.

What conditions does trial NCT06411990 study?

This clinical trial studies the following conditions: Aortic Aneurysm, Endovascular Aneurysm Repair. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06411990?

The interventions under investigation include: Fenestrated Endovascular Aneurysm Repair using the LIFE Device System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06411990?

This trial is sponsored by Jonathan Bath, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06411990 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial