Positron Emission Tomography Using [18F]-Labeled Substance P Antagonist Receptor Quantifier in Finding Disease in Patients With Pancreatic Cancer
Completed · Phase 1
Conditions studied: Pancreatic Cancer
In brief
RATIONALE: Diagnostic procedures, such as positron emission tomography (PET) using \[18F\]-labeled substance P antagonist receptor quantifier, may be effective in finding disease in patients with pancreatic cancer. PURPOSE: This phase I trial is studying how well a PET scan using \[18F\]-labeled substance P antagonist receptor quantifier works in finding disease in patients with pancreatic cancer.
Key facts
- Study ID
- NCT00547612
- Run by
- National Institutes of Health Clinical Center (CC)
- People needed
- 33
- Starts
- 2007-09-01
- Expected to finish
- 2008-12-01
- Last updated by the study team
- 2012-03-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- ECOG performance status 0-2
- WBC ≥ 1,200/mm³
- Creatinine < 2.0 mg/dL
- Negative pregnancy test
- Fertile patients must agree to use effective contraception
- Not pregnant or nursing
You may not qualify if…
- Allergy to IV contrast
- Claustrophobia that would preclude completion of a scan or unable to lie on one's back for positron emission tomography scan
- PRIOR CONCURRENT THERAPY:
- Inclusion criteria:
- More than 4 weeks since prior abdominal surgery
- Exclusion criteria:
- Prior participation in other research protocols within the past year such that a radiation exposure together with the present study would exceed the annual limits
- Aprepitant within 72 hours of [18F]-labeled substance P antagonist receptor quantifier positron emission tomography
Where it is running
- Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office — Bethesda, Maryland, United States
Full record on ClinicalTrials.gov
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