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Sponsored by: |
University of California, Los Angeles |
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Information provided by: | University of California, Los Angeles |
ClinicalTrials.gov Identifier: | NCT00351728 |
Patients diagnosed with ocular melanoma consent to participate in the study. Combined PET/CT scans of the whole body are performed at baseline, three months later, and six months after that for a total of three combined scans in the first year. Subsequently, these combined scans will be performed at 6-monthly intervals for a total of two combined scans per year.
Condition |
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Ocular Melanoma Choroidal Melanoma Uveal Melanoma |
Study Type: | Observational |
Study Design: | Longitudinal, Defined Population, Prospective Study |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | UCLA IRB #05-04-016 |
Study First Received: | July 12, 2006 |
Last Updated: | July 12, 2006 |
ClinicalTrials.gov Identifier: | NCT00351728 |
Health Authority: | United States: Institutional Review Board |
Ocular melanoma Neuroectodermal Tumors Uveal melanoma Intraocular melanoma Nevus, Pigmented Neoplasms, Germ Cell and Embryonal |
Neoplasm Metastasis Neuroepithelioma Nevus Melanoma of the choroid Neuroendocrine Tumors Melanoma |
Neoplasms Neoplasms by Histologic Type Neoplasms, Nerve Tissue Nevi and Melanomas |