Clinical Trials Directory

Trials / Terminated

TerminatedNCT00965861

SCRI Tissue Testing Registry

Status
Terminated
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
SCRI Development Innovations, LLC · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Detailed description

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).

Conditions

Interventions

TypeNameDescription
OTHERTissue Registry StudyIf 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.

Timeline

Start date
2010-05-01
Primary completion
2013-02-01
Completion
2013-02-01
First posted
2009-08-26
Last updated
2013-08-28

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00965861. Inclusion in this directory is not an endorsement.