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This study has been withdrawn prior to enrollment.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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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 August 28, 2014