Cone Beam CT Scanning in Lung and Bladder Cancer.
Improving the Accuracy of Radiotherapy Planning and Delivery Using Kilovoltage Cone Beam CT Imaging
1 other identifier
observational
22
1 country
1
Brief Summary
To study changes in tumor and normal organ size and/or position which occur during a course of radiation treatments.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started May 2007
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2007
CompletedFirst Submitted
Initial submission to the registry
May 2, 2007
CompletedFirst Posted
Study publicly available on registry
May 4, 2007
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2010
CompletedFebruary 24, 2016
December 1, 2011
2.3 years
May 2, 2007
February 23, 2016
Conditions
Keywords
Eligibility Criteria
primary care clniic
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- AHS Cancer Control Albertalead
- Cross Cancer Institutecollaborator
Study Sites (1)
Cross Cancer Institute
Edmonton, Alberta, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Don Yee, MD
AHS Cancer Control Alberta
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 2, 2007
First Posted
May 4, 2007
Study Start
May 1, 2007
Primary Completion
August 1, 2009
Study Completion
April 1, 2010
Last Updated
February 24, 2016
Record last verified: 2011-12