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Bolus of Saline in Stroke — BOSS  

Ischemic Stroke Clinical Trial

Official title:
Optical Measurement of Cerebral Blood Flow Response After Ischemic Stroke

Clinical Trial Summary

This study is a non-randomized, Phase 2 clinical trial designed to assess optical cerebral blood flow (CBF) response to bolus normal saline. Subjects will have had an ischemic stroke within 96 hours of enrollment. The study intervention will be a one hour monitoring session. There will be a 15 minute baseline measurement period, followed by intravenous administration of 500cc of 0.9% NaCl over 30 minutes, and finally 15 minutes of monitoring post-bolus. All study measurements will cease after 1 hour. Subjects will be followed during their hospitalization for 7 days or until discharge, whichever is sooner, to monitor for adverse events and to collect clinical information.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01971463
Study type Interventional
Source University of Pennsylvania
Contact
Status Completed
Phase Phase 2
Start date October 2013
Completion date September 2019
View Details
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