Clinical trial · Interventional
Dosimetric Planning Study Comparing Intensity Modulated Radiotherapy (IMRT) and 4-field Radiotherapy for Definitive Treatment of Cancer of the Cervix
Dosimetric Planning Study Comparing IMRT and 4-field Radiotherapy for Definitive Treatment of Cancer of the Cervix
NCT00981552CI-TRIAL-00002654completedEarly Phase 1ClinicalTrials.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)
A theoretical planning study to compare the normal tissue irradiation when using intensity modulated radiotherapy (IMRT) as opposed to standard radiotherapy for the definitive treatment of cervical cancer.
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 |
|---|---|---|---|
| Cervix Cancer | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 4-Field Radiation Planning | Radiation | — | UNRESOLVED |
| IMRT planning | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- OTHER
- label
- Cervix Cancer
- description
- Patients treated with cervical cancer in 2008 at Sunnybrook Odette Cancer Centre
- interventionNames
- Radiation: IMRT planning
- Radiation: 4-Field Radiation Planning
Primary outcomes (1)
- measure
- Reduction in dose to organs at risk
- timeFrame
- 6 months
Secondary outcomes (1)
- measure
- Target Coverage
- timeFrame
- 6 months
Eligibility
Eligibility (as posted)
- Sex
- Female
Show eligibility criteria text
Inclusion Criteria: * last 60 patients treated definitively for cervical cancer at Sunnybrook Odette Cancer Centre Exclusion Criteria: * no imaging and no anatomical description of disease
References
Publications (0)
Data not yet available
No reference posted for this study.