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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00469066
Other study ID # LU-11-0073
Secondary ID
Status Completed
Phase N/A
First received May 2, 2007
Last updated February 23, 2016
Start date May 2007
Est. completion date April 2010

Study information

Verified date December 2011
Source AHS Cancer Control Alberta
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Observational

Clinical Trial Summary

To study changes in tumor and normal organ size and/or position which occur during a course of radiation treatments.


Recruitment information / eligibility

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

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Locations

Country Name City State
Canada Cross Cancer Institute Edmonton Alberta

Sponsors (2)

Lead Sponsor Collaborator
AHS Cancer Control Alberta Cross Cancer Institute

Country where clinical trial is conducted

Canada, 

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