Thyroid Cancer Clinical Trial
Official title:
Comparison of I-124 PET/CT, F-18 FDG PET/CT and I-123 Whole Body Scintigraphy for Recurrent Thyroid Cancer Detection
NCT number | NCT00373711 |
Other study ID # | END0003 |
Secondary ID | 97454END0003 |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | May 2007 |
Verified date | April 2011 |
Source | Stanford University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The management of thyroid cancer patients with suspicion of recurrent disease based on rising/detectable levels of thyroglobulin (Tg) involves imaging with iodine-123 whole body scintigraphy (I-123 WBS) and F-18 FDG PET/CT. However, the disease is not always detected. The use of another iodine isotope (I-124) with positron emitting characteristics for PET/CT may allow better identification of recurrent disease, thus allowing for more patients to be treated with I-131 as a curative attempt.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria:- Patient at Nuclear Medicine clinic at Stanford University Medical Center - Treated thyroid cancer. - Detectable levels of Tg. - Referred for I-123 WBS and F-18 FDG PET/CT for detection of recurrent thyroid cancer. - Able to have a I-124 PET/CT the day after I-123 WBS and F-18 FDG PET/CT - Patients older than 18-year-old. - Patients with history of treated thyroid cancer and suspected recurrent thyroid cancer based on detectable levels of Tg. - Patients must have I-123 WBS and F-18 FDG PET/CT performed prior to the I-124 PET/CT. - Patients must understand and voluntarily sign an Informed Consent form after the contents have been fully explained to them. Exclusion Criteria:- Patients who are not eligible for I-123 WBS and F-18 FDG PET/CT. - Patients who cannot complete I-123 WBS and F-18 FDG PET/CT. - Pregnant women. - Healthy volunteers. - Patients participating in other research studies. |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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Stanford University |
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