Performance of 18F-FDG Micro-PET-CT in the Assessment of Surgical Margins in Head and Neck Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Henri Becquerel

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

Qualifiers

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

Treatments tested in this trial

  • micro PET/CT

Treatment groups

10 Participants
are divided into 1 treatment group

Sponsors and collaborators