Actively Recruiting

Age: 18Years +
All Genders
NCT06970275

To Assess the Correlation of High-resolution Specimen PET-CT Imaging, Using the XEOS AURA 10 PET-CT, With the Histopathology Results and Long-term Outcome of Patients Undergoing Resective Cancer Surgery.

Led by XEOS Medical · Updated on 2025-12-05

850

Participants Needed

1

Research Sites

269 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This registry study aims to evaluate the effectiveness and clinical impact of specimen PET-CT imaging by analyzing the correlation between specimen PET-CT images, intraoperative interpretations, and histopathological findings. Additionally, it assesses how these imaging insights influence clinical decision-making and long-term patient outcomes. Through this comprehensive analysis in a real-world setting, the study seeks to generate valuable insights that can enhance specimen evaluation processes and ultimately improve patient care.

CONDITIONS

Official Title

To Assess the Correlation of High-resolution Specimen PET-CT Imaging, Using the XEOS AURA 10 PET-CT, With the Histopathology Results and Long-term Outcome of Patients Undergoing Resective Cancer Surgery.

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for surgery to remove cancerous tissue with PET-CT imaging performed on their specimens using the AURA 10 PET-CT
  • Successful PET-CT imaging includes having at least part of the primary tumor visible, correct radiotracer injection, and interpretable images without technical issues
  • Patients willing to provide informed consent for use of their medical records
  • Retrospective patients included if no further long-term follow-up is needed
Not Eligible

You will not qualify if you...

  • Patients younger than 18 years at the time of surgery
  • Women who are pregnant or breastfeeding

AI-Screening

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Trial Site Locations

Total: 1 location

1

AZ Maria Middelares

Ghent, Belgium

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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