Clinical Trials Directory

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

TypeNameDescription
RADIATIONIMRT planning
RADIATION4-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.