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Clinical Trial Summary

The overall aim of the registry is to develop a longitudinal, observational database that is focused on adult patients with Normal Pressure Hydrocephalus (NPH) that can be used as a source of clinical information for individual surgeons, as well as a national data repository for scientific inquiry and publications.


Clinical Trial Description

This is a prospective, multi-center, observational database to collect data on the characteristics, management practices, and patient outcomes of NPH patients. It will be offered to a geographically representative group of U.S. physicians who will enroll NPH patients. The physician makes his/her own clinical decisions; thus, the data captured provides current practice patterns related to diagnosis, management, and results. The registry may also assist physicians in patient follow-up and certain practice management tasks. The data collected will serve to inform the medical community on optimal care for this patient population ;


Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT00233701
Study type Observational
Source Codman & Shurtleff
Contact
Status Completed
Phase Phase 4
Start date October 2004
Completion date September 2008

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