Trials / Completed
CompletedNCT00981552
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
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 55 (actual)
- Sponsor
- Sunnybrook Health Sciences Centre · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
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.
Detailed description
Radiotherapy in combination with chemotherapy is the standard treatment of locally advanced cervix cancer, however with traditional techniques large volumes of bowel and bladder are irradiated causing short-term and long-term genito-urinary and gastro-intestinal side effects. IMRT has the potential to conform precisely to the target and spare normal tissues and reduce side effects. However because there are large dose gradients there is the potential to miss the target due to organ motion. Recent studies have documented organ motion and will be used to define the target. Approximately 60 planning scans, previously used to treat patients with cervix cancer, will be used to replan using an IMRT technique and differences in doses to tumour and normal tissues compared.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| RADIATION | IMRT planning | |
| RADIATION | 4-Field Radiation Planning |
Timeline
- Start date
- 2008-12-01
- Primary completion
- 2009-07-01
- Completion
- 2009-09-01
- First posted
- 2009-09-22
- Last updated
- 2009-09-22
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT00981552. Inclusion in this directory is not an endorsement.