MedPath

Validation of FDG-PET Segmentation Tools for Tumor Delineation by Correlation of CT- and FDG-PET Volume Measurements With Histopathology of Nodal Metastases of Head and Neck Carcinomas.

Conditions
Head and Neck Cancer
Registration Number
NCT00782691
Lead Sponsor
Radboud University Medical Center
Brief Summary

Various methods of FDG-PET signal segmentation will be validated by correlation of histopathologically measured tumor dimensions in lymph node dissection specimens of head-and-neck cancer patients.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
15
Inclusion Criteria
  • All patients with N+ squamous cell carcinoma of the head and neck, planned for neck dissection.
  • Age >18 years.
Exclusion Criteria
  • Pregnancy.
  • Women breast feeding

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
How accurate are the various FDG-PET segmentation tools?Measurements are performed in conjunction with the clinical pathologist directly postoperatively.
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Radboud University Nijmegen Medical Centre

🇳🇱

Nijmegen, Gelderland, Netherlands

Radboud University Nijmegen Medical Centre
🇳🇱Nijmegen, Gelderland, Netherlands
Dominic AX Schinagl, MD
Principal Investigator

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.