Diagnostic Accuracy of ShuntCheck Compared to Radionuclide Shunt: Patency in Patients With Normal Pressure Hydrocephalus

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40+
SponsorUniversity of South Florida

About this trial

The purpose of this study is to assess the diagnostic accuracy of ShuntCheck compared with radionuclide shunt patency testing (SPS) to detect CSF shunt flow of NPH patients with suspected shunt obstruction.

Eligibility criteria

Qualifiers

Men or women 40 yo or older and have a VP shunt placed for NPH and are suspected of shunt obstruction.

Capable of providing valid signed informed consent, or has a legal guardian, health care agent, or surrogate decision maker (according to local statutes, and collectively referred to as "surrogates" in this protocol) capable of providing valid, signed informed consent

Disqualifiers

Presence of multiple shunts, or presence of more than one distal shunt catheter (regardless of function) crossing the clavicle ipsilateral to the shunt with suspected obstruction;

ShuntCheck test would interfere with standard patient care, or emergency shunt surgery that cannot be delayed is indicated;

Presence of an interfering open wound or edema over any portion of the VP shunt.

Trial design

Treatments tested in this trial

  • ShuntCheck

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of South Florida

Lead sponsor

NeuroDx Development

Collaborator