Study to Test Sensitivity and Specificity of Passive Wave Pressure Device in Determining Ischemic Stroke
Stopped early
Conditions studied: Ischemic Stroke
In brief
That the Jan Medical Nautilus NeuroWaveTM system provides significantly higher sensitivity to hyper acute ischemic stroke than does CT.
Key facts
- Study ID
- NCT01643525
- Run by
- Jan Medical, Inc.
- People needed
- 29
- Starts
- 2012-06-01
- Expected to finish
- 2012-12-01
- Last updated by the study team
- 2024-07-08
Who can join
Age: 18 and older, up to 90. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Symptoms consistent with stroke with known onset < 12 hours prior to enrollment and planned recording with the Nautilus NeuroWave System
- Suspected pathology of following vessels: internal carotid artery, ACA, MCA, PCA, basilar or other anterior or posterior cerebral vessels or normal anatomy
- Subject is planned to undergo standard stroke triage imaging protocol
- Able to understand and provide signed informed consent, or have a Legally Authorized Representative willing to provide informed consent on subject's behalf
You may not qualify if…
- Known to meet hospital criteria for brain death
- Not a candidate for CT, MRI
- unknown time of stroke symptom onset.
- Psychologically unstable and not able to cooperate
- Not suitable for participation in this study in the opinion of the Investigator
Where it is running
- Johns Hopkins Hospital — Baltimore, Maryland, United States
- Johns Hopkins Bayview Medical Center — Baltimore, Maryland, United States
- Howard County General Hospital — Columbia, Maryland, United States
Full record on ClinicalTrials.gov
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