About this trial
The purpose of this study is to evaluate the diagnostic performance of 18F-FDG micro-PET-CT in malignant Head and neck cancer compared to definitive histological analysis (gold standard).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Signed informed consent
Adult, male or female, aged 18 or over
Patient with a malignant tumor of the oral cavity, oropharynx, hypopharynx, larynx, sinuses, or salivary glands, regardless of lymph node status (any N) M0, operable
Member or beneficiary of a social security plan
Disqualifiers
Child-Pugh C liver failure
Patients under guardianship, conservatorship, or legal protection
Patients deprived of their liberty
Pregnant or breastfeeding women
Trial design
Single group
Treatments tested in this trial
micro PET/CT
DevicePET/T of the speciment after surgery
Treatment groups
Trial outcomes
Primary outcomes
Evaluate the diagnostic performance of 18F-FDG micro-PET-CT in malignant ENT tumors compared to definitive histological analysis (gold standard).
Estimate the performance of micro-FDG PET in defining surgical margins and compare with histology by measuring the number of quadrants affected by each technique on the surgical specimen
Sponsors and contacts
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