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Clinical Trials/NCT00767273
NCT00767273
Completed
Not Applicable

Pilot Study to Investigate the Role of Metabolic Imaging in Predicting Tumor Response and Outcome After Therapy for Pancreatic Cancer

Stanford University1 site in 1 country30 target enrollmentOctober 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pancreatic Cancer
Sponsor
Stanford University
Enrollment
30
Locations
1
Primary Endpoint
Evaluate the performance of the novel imaging methods
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

To test the ability of new imaging techniques to monitor and predict response of pancreatic cancer to radiation and/or chemotherapy.

Registry
clinicaltrials.gov
Start Date
October 2006
End Date
December 2007
Last Updated
13 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Albert Koong

Associate Professor of Radiation Oncology

Stanford University

Eligibility Criteria

Inclusion Criteria

  • Adult patients (\>18) with histologically confirmed adenocarcinomas of the pancreas with a - treatment plan consisting of definitive or palliative radiation therapy and/or chemotherapy with or without surgery.
  • Negative urine pregnancy test if a woman of child-bearing potential (WOCBP).
  • WOCBP must be using an adequate method of contraception to avoid pregnancy throughout the study period.
  • All patients will be evaluated in a uniform manner at the Stanford GI Combined Modality Tumor Board to determine eligibility.

Exclusion Criteria

  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • Any concurrent malignancy other than non-melanomaskin cancer, or carcinomainsitu of the cervix. Patients with a previous malignancy without evidence of disease for \>5 years will be allowed to enter the trial.
  • WOCBP who is pregnant or breastfeeding.
  • Inability to sign written consent.

Outcomes

Primary Outcomes

Evaluate the performance of the novel imaging methods

Secondary Outcomes

  • Correlate FLT activity with clinical outcomes

Study Sites (1)

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