Feasibility of Imaging in the Treatment of Patients With Advanced Head and Neck Cancer
Completed · Early Phase 1
Conditions studied: Head and Neck Cancer
In brief
The purpose of this study is to obtain preliminary information on the potential of 99m Tc-EC-DG SPECT imaging to distinguish cancer from non cancer.
Key facts
- Study ID
- NCT01359267
- Run by
- University of Chicago
- People needed
- 12
- Starts
- 2011-04-19
- Expected to finish
- 2015-09-15
- Last updated by the study team
- 2020-05-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Treatment naive patients with histologically proven cancer of the head and neck
- T4 primary tumor (all sites), N2 or N3 locoregional disease (all sites)
- At least one measurable site of disease
- At least 18 years of age
- Karnofsky performance status > or = 70% or ECOG <2
- Able to tolerate SPECT/CT imaging
- Adequate bone marrow function
- Adequate liver function
- Adequate renal function
- Written consent from patients
- Female patients of childbearing potential must have a negative pregnancy test within 0-7 days prior to the first SPECT study
You may not qualify if…
- Diabetics with insulin dependence or blood sugar levels >200 mg/dL prior to imaging
- Patient weight above the SPECT/CT table weight limit
- Pregnant and/or lactating female
- Unequivocal demonstration of metastatic disease
- Patients unwilling to or unable to comply with protocol
Where it is running
- University of Chicago — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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