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Protocol No. UW19056

Principal Investigator Jeraj, Robert

Phase N/A

Age Group Adult

Scope Local

Sponsor Type Institutional

Title Determining FDG PET/CT Repeatability in Patients with Solid Tumor

Objective The purpose of this study is to determine if the same results are produced in two separate FDG PET/CT imaging sessions. The first FDG PET/CT imaging session is part of you standard clinical care ordered by your doctor

Treatment You will be asked to complete 1 study visits that will include a PET/CT scan, then you will undergo a second FDG PET/CT scan (baseline #2) within 2 weeks of the initial scan to determine repeatability of FDG PET/CT scanning

Description Determining FDG PET/CT repeatability in patients with solid tumors

Key Eligibility
  • Patients with an identifiable malignancy. Note: Preference will be given to subjects with multiple lesions that can be imaged in one image acquisition session to obtain maximal information
  • Men and women of age 18 years or older
  • Women must not be pregnant
  • Patients must be able to comply with all study procedures, including having both the ability and willingness to lie flat for ≥ 30 minutes during imaging
  • Patients must have both the ability to understand and the willingness to sign a written informed consent document
    Exclusion Criteria:
  • Concurrent treatment with any agent that is being used with the expressed purpose of treating cancer
  • Patients who have received radiotherapy less than 2 weeks prior to registration
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to 18F-fludeoxyglucose (FDG

  • Applicable Disease Sites Anal; Any Site; Bladder; Brain/Central Nervous System; Breast; Cervix; Colon and Rectum; Endocrine cancers; Esophagus; Gastrointestinal cancers, other; Genitourinary cancers, other; Head and Neck; Ill-Defined Sites; Kidney; Liver; Lung; Melanoma/Skin cancer; Ovary; Pancreas; Prostate; Sarcoma; Stomach; Thyroid; Unknown Sites; Uterus

    Status Open