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
Interventions
Other: CT-FDG/PET scan of the head-and-neck region
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
Arm && Interventions
GroupInterventionDescription
Head-and-neck cancer patients.CT-FDG/PET scan of the head-and-neck regionHead-and-neck cancer patients eligible for therapeutic lymph node dissection of cervical nodes.
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

© Copyright 2025. All Rights Reserved by MedPath