Clinical trial · Interventional
Effect of FDG-PET/CT for Simulation and Radiation Treatment Planning in Oral Cancer Patients
Phrase II Single Arm Study of Effect of FDG-PET/CT for Simulation and Radiation Treatment Planning in Oral
NCT03008694CI-TRIAL-00025319unknownPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study evaluates the effect of FDG-PET/CT for Simulation and Radiation Treatment Planning in oral Cancer patients. Progress-free survival (PFS) will be compared with historical control as defined in the protocol
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Oral Cancer | Malignant Lip and Oral Cavity Neoplasm | CURATED_BROADER | 0.80 |
| Radiotherapy; Complications | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| PET/CT | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- 1
- description
- PET/CT
- interventionNames
- Device: PET/CT
Primary outcomes (1)
- measure
- progress free survival
- timeFrame
- baseline to 2 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Histologically confirmed oral squamous-cell carcinoma * Age \> 17 years * Signed informed consent * ECOG Performance status 0-2 * Must be able to start RT within 4 weeks after PET/CT simulation Exclusion Criteria: * stage IV disease diagnosed before acquisition of staging PET/CT * prior radiotherapy to oral and neck * Unable to understand study participation * Claustrophobia * pregnant or breast feeding mothers
References
Publications (0)
Data not yet available
No reference posted for this study.