Clinical trial · Observational
Planning Margin Requirements for Pediatric Radiation Oncology
NCT00704613CI-TRIAL-00005849completedClinicalTrials.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)
The planning target volume (PTV) and planning organ at risk volume (PRV) margins used for pediatric radiation therapy are empiric, and quantitative assessment of these margins is needed to improve therapy planning and delivery.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Pediatric Radiation | — | UNRESOLVED | — |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Acquire data to develop setup margin (SM) portion of the planning target volume (PTV) margin for pediatric tumor sites according to age, localization technique, treatment position, and the use of general anesthesia.
- timeFrame
- 4 year
Secondary outcomes (1)
- measure
- Estimate the number of patients required to develop a patient specific PTV and RTV margin recommendations.
- timeFrame
- 4 year
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: * Patients will receive conformal or intensity-modulated radiation therapy (3D or IMRT). * Research participant or legal guardian/representative gives written informed consent. Exclusion Criteria: * Unwillingness of research participant or legal guardian/representative to give written informed consent
References
Publications (0)
Data not yet available
No reference posted for this study.