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Clinical Trials/NCT00725387
NCT00725387
Completed
Not Applicable

Combined F-18 NaF and F-18 FDG PET/CT for Evaluation of Malignancy

Stanford University5 sites in 5 countries214 target enrollmentAugust 2007
ConditionsNeoplasms

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Neoplasms
Sponsor
Stanford University
Enrollment
214
Locations
5
Primary Endpoint
Percent of patients with evidence of new lesions on combined F-18/F-18 FDG PET/CT.
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Fluorine-18 Fluorodeoxyglucose (F-18 FDG) PET/CT is established as a powerful imaging tool for cancer detection and monitoring response to therapy. Sodium Fluorine-18 (F-18) was used in the 1970s for bone scanning and can be used as a skeletal tracer in current PET/CT scanners. The combined administration of F-18 and F-18 FDG in a single PET/CT scan for cancer detection was not attempted to date. We hope to learn what is the best approach for detection of cancer and thus to improve cancer treatment.

Registry
clinicaltrials.gov
Start Date
August 2007
End Date
June 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients older than 18-year-old, diagnosed with cancer
  • Patients must understand and voluntarily sign an Informed Consent form after the contents have been fully explained to them

Exclusion Criteria

  • Patients who cannot complete a PET/CT scan
  • Pregnant women
  • Healthy volunteers
  • Patients participating in other research studies
  • The subjects will not be paid to participate in this protocol. No costs will be charged to the subjects.

Outcomes

Primary Outcomes

Percent of patients with evidence of new lesions on combined F-18/F-18 FDG PET/CT.

Time Frame: not defined

Study Sites (5)

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