Multi-Center Study of ShuntCheck

This study has been withdrawn prior to enrollment.
(Insufficient funding)
Sponsor:
Information provided by:
NeuroDx Development
ClinicalTrials.gov Identifier:
NCT00788385
First received: November 7, 2008
Last updated: November 19, 2009
Last verified: November 2009
  Purpose

Multi-Center Study of ShuntCheck


Condition Intervention Phase
Blocked Ventricular Shunts
Device: ShuntCheck test
Phase 4

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Diagnostic
Official Title: Multi-Center Study of ShuntCheck

Resource links provided by NLM:


Further study details as provided by NeuroDx Development:

Estimated Enrollment: 350
Study Start Date: June 2009
Estimated Study Completion Date: December 2010
Estimated Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   1 Month to 19 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

Exclusion Criteria:

  Contacts and Locations
No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Fred Fritz, Neuro Diagnostic Devices
ClinicalTrials.gov Identifier: NCT00788385     History of Changes
Other Study ID Numbers: NDX01-22-2001
Study First Received: November 7, 2008
Last Updated: November 19, 2009
Health Authority: United States: Institutional Review Board

Keywords provided by NeuroDx Development:
Hydrocephalus
High Pressure
Shunt Blockage

ClinicalTrials.gov processed this record on April 15, 2014