Trial Information
A Longitudinal Study of Biomarkers in Pediatric Patients With Central Nervous System Tumors
Inclusion Criteria:
- Patients ages 1 day to 21 years
- Patients with radiographically and/or histologically confirmed CNS tumors treated at
Children's Memorial Hospital and Lurie Children's Hospital in Chicago
- Patients must be newly diagnosed and have had no prior anticancer therapy (except
surgery) for their current diagnosis. The use of steroids is permissible.
- Patients and/or parents/legal guardians must have signed an informed consent and
assent when applicable.
Exclusion Criteria:
- Patients who have completed treatment and do not require routine blood draws and/or
lumbar punctures
- Patients who are considered too ill to participate as determined by their treating
physician
- Patients who are pregnant or lactating
Type of Study:
Observational
Study Design:
Observational Model: Case-Only, Time Perspective: Prospective
Outcome Measure:
Presence of microRNAs and proteins in the blood, cerebrospinal fluid and urine of patients with central nervous system tumors from diagnosis through the course of their treatment
Outcome Time Frame:
24 months
Safety Issue:
No
Principal Investigator
Rishi Lulla, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Ann & Robert H Lurie Children's Hospital of Chicago
Authority:
United States: Institutional Review Board
Study ID:
2012-14877
NCT ID:
NCT01595126
Start Date:
December 2011
Completion Date:
Related Keywords:
- Central Nervous System Tumor
- Nervous System Neoplasms
- Central Nervous System Neoplasms
Name | Location |
Children's Memorial Hospital |
Chicago, Illinois 60614 |