Observational study of a wireless skin device (FlowSense) to detect blocked cerebrospinal fluid shunts

You may qualify if

• Existing ventriculoperitoneal CSF shunt on which the subject is dependent
• At least one symptom of shunt malfunction as determined by the investigator, such as but not limited to seizure, fever, headache, vision problems, dizziness, disorientation, confusion, vomiting, lethargy, irritability, difficulty waking or staying awake, swelling along shunt tract, enlargement of head, loss of balance, gait disturbance, and loss of sensory or motor function
• Exhibit shunt malfunction symptom(s) requiring surgical shunt revision per standard of care assessment without use of device data
• Region of intact skin overlying an unambiguously identifiable chronically indwelling ventricular shunt which crosses the clavicle and is appropriate in size for application of the study device
• Available for follow-up for up to seven days
• Signed informed consent by subject or a parent, legal guardian, health care agent, or surrogate decision maker (according to local statutes, and collectively referred to as "surrogates" in this protocol)

You can't join if

• Presence of more than one distal shunt catheter in the study device measurement region
• Presence of an interfering open wound or edema in the study device measurement area
• Subject-reported history of adverse skin reactions to adhesives
• Investigator judges that the subject is likely to be lost to follow-up due to unavailability or clinical outcome being unobtainable
• Participation in the study will interfere with, or be detrimental to, administration of optimal health-care to the subject
• Previous participation in a Rhaeos clinical study in which FlowSense device measurement data were acquired
• Participation in any other investigational procedural, pharmaceutical, and/or device study that may influence the collection of valid data under this study