Lung Neoplasm Clinical Trial
Official title:
Improving the Accuracy of Radiotherapy Planning and Delivery Using Kilovoltage Cone Beam CT Imaging
| Verified date | December 2011 |
| Source | AHS Cancer Control Alberta |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Canada: Health Canada |
| Study type | Observational |
To study changes in tumor and normal organ size and/or position which occur during a course of radiation treatments.
| Status | Completed |
| Enrollment | 22 |
| Est. completion date | April 2010 |
| Est. primary completion date | August 2009 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - Patient has biopsy proven limited stage SCLC - receiving radical concurrent chemoradiotherapy - no prior chest RT - no prior surgical resection of lung tumor - no prior chemotherapy - patients' lung tumors should be centrally-located to minimize the effect of respiratory motion - patient has biopsy proven TCC bladder - receiving radical concurrent chemoradiotherapy or RT alone - no prior chemotherapy - patient signs study-specific consent form Exclusion Criteria: - mixed small cell and non small cell histology - patient not being treated with concurrent chemoradiotherapy - chemoradiotherapy given sequentially - previous chest RT - previous chemotherapy - prior surgical resection of lung mass - patient ineligible for pelvic RT - patient does not sign study consent |
Observational Model: Case-Only, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Canada | Cross Cancer Institute | Edmonton | Alberta |
| Lead Sponsor | Collaborator |
|---|---|
| AHS Cancer Control Alberta | Cross Cancer Institute |
Canada,
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