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RECRUITING

ViTAA Registry Pre- and Post-Operative Monitoring for Endovascular Aortic Aneurysm Repair and Serial Monitoring for AAA

NCT05004051 · View on ClinicalTrials.gov ↗

Study Summary

This is a Prospective Registry study to collect imaging and clinical data both on patients with aortic aneurysm disease undergoing serial monitoring and on patients pre and post-endovascular repair, using ViTAA (The Sponsor) aortic mapping technology.

Conditions Studied

Interventions

  • DEVICE ViTAA Analysis

Study Locations (8)

Quebec

  • CHUM - Centre Hospitalier de l'Université de Montréal — Montreal
  • MUHC - McGill University Health Centre — Montreal

Alabama

  • UAB - University of Alabama in Birmingham Hospital — Birmingham

Massachusetts

  • MGH - Massachusetts General Hospital Fireman Vascular Center — Boston

North Carolina

  • UNC - University of North Carolina at Chapel Hill — Chapel Hill

Washington

  • University of Washington — Seattle

Alberta

  • UCGY - University of Calgary, Peter Lougheed Center — Calgary

Ontario

  • UHN - University Health Network - Toronto General Hospital — Toronto

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2021-12-15
Est. Completion 2026-12-31

Sponsor

ViTAA Medical Solutions

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05004051

The ClinicalTrials.gov registry entry for NCT05004051 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ViTAA Medical Solutions, 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 1 condition, with Abdominal Aortic Aneurysms appearing as the primary indexed condition, and to 1 intervention — of which ViTAA Analysis 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: NCT05004051 reports 8 study locations spanning 7 distinct geographic areas — top geographies include Quebec, Alabama, Massachusetts. 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 NCT05004051 about?

NCT05004051 is a clinical study titled "ViTAA Registry Pre- and Post-Operative Monitoring for Endovascular Aortic Aneurysm Repair and Serial Monitoring for AAA". This is a Prospective Registry study to collect imaging and clinical data both on patients with aortic aneurysm disease undergoing serial monitoring and on patients pre and post-endovascular repair, using ViTAA (The Sponsor) aortic mapping technology.

What is the current status of trial NCT05004051?

This trial is currently recruiting. The enrollment target is 200 participants. The study started on 2021-12-15. Estimated completion is 2026-12-31.

What conditions does trial NCT05004051 study?

This clinical trial studies the following conditions: Abdominal Aortic Aneurysms. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05004051?

The interventions under investigation include: ViTAA Analysis (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05004051?

This trial is sponsored by ViTAA Medical Solutions, 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 NCT05004051 being conducted?

This trial has 8 study locations across Alabama, Massachusetts, North Carolina, Washington, Alberta. 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