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Clinical Trial Summary

The purpose of this study is to evaluate the sensitivity and specificity of "A-PROTEIN" levels in patients with brain tumors. A-PROTEIN levels will be analyzed both pre and post treatment. Levels in blood and/or cerebrospinal fluid (CSF) will be analyzed and correlated with the underlying diagnosis and outcome.


Clinical Trial Description

- Patients will be identified at the time of presentation to their neurologist, neurosurgeon or oncologist.

- Blood or cerebrospinal fluid will be collected for this study only when they are being collected for other reasons before and after each surgery. Samples will also be collected after any event such as significant change in symptoms or radiographic progression.

- Once the patients condition has been stabilized, samples will be take at regular intervals of >= 1 month. The duration of this study is 24 months. ;


Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00165542
Study type Observational
Source Dana-Farber Cancer Institute
Contact
Status Completed
Phase N/A
Start date June 1998
Completion date August 2009