The objective of this feasibility study is to demonstrate the safety and feasibility of using an investigational extracorporeal system and catheter to filter hemorrhagic cerebrospinal fluid (CSF) post subarachnoid hemorrhage (SAH) treatment, and reintroduce the CSF via the same catheter.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
15
Extracorporeal filtration of CSF
University of Minnesota
Minneapolis, Minnesota, United States
Duke University
Durham, North Carolina, United States
Thomas Jefferson University
Philadelphia, Pennsylvania, United States
Memorial Hermann
Houston, Texas, United States
Device/System Safety - Adverse events related to the filtration procedure
Adverse events related to the filtration procedure
Time frame: 30 days
Adverse events related to the system catheter insertion
Nerve or tissue damage related to catheter insertion
Time frame: 30 days
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