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Diagnostic Performance Of 4D Dynamic LAFOV FDG-PET Acquisition for Differentiation of Resi

This multicenter prospective observational study will evaluate the value of dynamic FDG-PET LAFOV imaging during the initial therapeutic assessment of a head and neck cancer 3 months after completion of curative radiotherapy.

Condition(s)Head & Neck Squamous Cell Carcinoma
StatusRecruiting
Study typeObservational
SummaryThis multicenter prospective observational study will evaluate the value of dynamic FDG-PET LAFOV imaging during the initial therapeutic assessment of a head and neck cancer 3 months after completion of curative radiotherapy.
Who can participateInclusion Criteria: * Adult patient ≥ 18 years of age * Presenting with head and neck squamous cell carcinoma * Completed curative treatment with external radiation therapy * Eligible for dynamic LAFOV FDG-PET scan for therapeutic evaluation at 3 months * Having given consent for the end-of-treatment consultation Exclusion Criteria: * Hypersensitivity to 18F-FDG or other excipients contained in the contrast agent * Pregnancy or breastfeeding * History of treated upper gastrointestinal tract cancer * Other histology * Incomplete RTE treatment regimen * Refusal to participate
Ages18 Years
SexAll
Lead sponsorUniversity Hospital, Brest
LocationsBrest, France
Start date2026-04-13
NCT IDNCT07417605
Official listinghttps://clinicaltrials.gov/study/NCT07417605

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