Metabolic Imaging Predict Histopathologic Response to Preop ChemoXRT for Locally Advanced Rectal CA

This study has been terminated.
(Protocol approval expired)
Stanford Cancer Council
Information provided by:
Stanford University Identifier:
First received: July 5, 2006
Last updated: March 25, 2010
Last verified: March 2010
In this research study of metabolic imaging in locally advanced rectal cancer, we hope to learn whether new medical imaging technology can help predict the response of rectal cancer to preoperative chemotherapy and radiation therapy. Ultimately we hope this information will in the future help us predict which patients will benefit from more or less aggressive initial therapy for their rectal cancer.

Condition Intervention
Rectal Cancer
Procedure: Metabolic Imaging

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Metabolic Imaging: Predicting Histopathologic Response to Preoperative Chemoradiotherapy for Locally Advanced Rectal Cancer

Resource links provided by NLM:

Further study details as provided by Stanford University:

Primary Outcome Measures:
  • 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 ] [ Designated as safety issue: No ]

Estimated Enrollment: 15
Study Start Date: October 2003
Study Completion Date: October 2005
Primary Completion Date: October 2005 (Final data collection date for primary outcome measure)

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

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.

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00394615

United States, California
Stanford University School of Medicine
Stanford, California, United States, 94305
Sponsors and Collaborators
Stanford University
Stanford Cancer Council
Principal Investigator: Albert Koong Stanford University
  More Information

Responsible Party: Albert Koong, Stanford University School of Medicine Identifier: NCT00394615     History of Changes
Other Study ID Numbers: REC0001 
Study First Received: July 5, 2006
Last Updated: March 25, 2010
Health Authority: United States: Institutional Review Board processed this record on May 02, 2016