SCRI Tissue Testing Registry
|ClinicalTrials.gov Identifier: NCT00965861|
Recruitment Status : Terminated (Replaced by a study with a similar design.)
First Posted : August 26, 2009
Last Update Posted : August 28, 2013
|Condition or disease||Intervention/treatment|
|Melanoma Myelodysplastic Syndrome Multiple Myeloma Lymphoma||Other: Tissue Registry Study|
Sarah Cannon Research Institute (SCRI) is committed to improvement and excellence in clinical research and correlative science. To this end, the SCRI Oncology Research Consortium will collect written consent from patients allowing the use of their tumor tissue sample(s) for testing/analysis at a future date. Future testing may include assays for newly identified markers of potential prognostic and/or therapeutic value. These markers may be specific to an individual cancer type, or they may be present more generally in cancer and/or other conditions.
This study will consist of a registry of patients who have agreed to allow their tissue sample(s) (even those taken prior to their participation in an SCRI-sponsored trial) to be used by the SCRI Oncology Research Consortium at some point in the future for testing and analysis of expression analysis and/or analysis of tumor markers. The registry will be contained in an electronic database, and will be sorted by disease indication. (Note: Patients will not be asked to return at a future date and have tissue samples collected; rather, SCRI will have the authorization to obtain pre-existing samples).
|Study Type :||Observational|
|Actual Enrollment :||20 participants|
|Official Title:||SCRI Tissue Testing Registry|
|Study Start Date :||May 2010|
|Primary Completion Date :||February 2013|
|Study Completion Date :||February 2013|
The SCRI Oncology Research Consortium will collect written consent from patients allowing the use of their tumor tissue sample(s) for testing/analysis at a future date.
Other: Tissue Registry Study
If a patient consents to allowing the use of their tumor tissue sample(s) for testing/analysis at a future date, their name and information will be stored electronically in a registry that will be managed by SCRI. SCRI may then use the information contained in this registry (such as disease indication, demographic information, etc.) at any time in the future to select tissue samples on which to perform testing/analyses.
- To establish an electronic registry to store information from patients who have provided their consent allowing use of their tissue sample(s) for future testing. [ Time Frame: 120 months ]
- To perform testing on the tissue samples to learn more about specific types of cancer and/or other diseases [ Time Frame: 120 months ]
Biospecimen Retention: Samples With DNA
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00965861
|United States, Tennessee|
|Tennessee Oncology, PLLC|
|Nashville, Tennessee, United States, 37023|
|Study Chair:||Howard Burris, M.D.||SCRI Development Innovations, LLC|