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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00394615
Date of registration: 05/07/2006
Primary sponsor: Stanford University
Public title: Metabolic Imaging Predict Histopathologic Response to Preop ChemoXRT for Locally Advanced Rectal CA
Scientific title: Metabolic Imaging: Predicting Histopathologic Response to Preoperative Chemoradiotherapy for Locally Advanced Rectal Cancer
Date of first enrolment: October 2003
Target sample size: 15
Recruitment status: Terminated
URL:  http://clinicaltrials.gov/show/NCT00394615
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment  
Countries of recruitment
United States
Contacts
Name:   Albert Koong
Address: 
Telephone:
Email:
Affiliation:  Stanford University
Key inclusion & exclusion criteria

Inclusion Criteria:- You must be diagnosed with locally advanced rectal cancer and have
chosen treatment with preoperative chemoradiotherapy followed by surgery, which is a
standard treatment approach for this disease.

Exclusion Criteria:- You are ineligible for this study if you are pregnant or under the
age of 18 years old.



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Rectal Cancer
Intervention(s)
Procedure: Metabolic Imaging
Primary Outcome(s)
To learn whether new medical imaging technology can help predict the response of rectal cancer to preoperative chemotherapy and radiation therapy. [Time Frame: not known]
Secondary Outcome(s)
Secondary ID(s)
REC0001
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Stanford Cancer Council
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