Normal Pressure Hydrocephalus (NPH) Registry

Completed

Conditions studied: Normal Pressure Hydrocephalus

In brief

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.

Key facts

Study ID

NCT00233701

Run by

Codman & Shurtleff

People needed

343

Starts

2004-10-01

Expected to finish

2008-09-01

Last updated by the study team

2010-02-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient meets the diagnosis criteria for Normal Pressure Hydrocephalus
• Patient is a candidate for a hydrocephalus shunt system, per the discretion of the investigator
• Patient or legal representative has signed an informed consent form. Competency to sign the consent form will be left up to the discretion of the investigator

You may not qualify if…

• Patient is under the age of 18 years
• Patient has a known contraindication for a shunt
• Patient has an expected life span of less than 24 months
• Patient has an unwillingness or inability to return for required follow-up visits

Where it is running

• Study site — Phoenix, Arizona, United States
• Study site — Los Angeles, California, United States
• Study site — Boulder, Colorado, United States
• Study site — Jacksonville, Florida, United States
• Study site — Macon, Georgia, United States
• Study site — Boise, Idaho, United States
• Study site — Chicago, Illinois, United States
• Study site — Iowa City, Iowa, United States
• Study site — Lexington, Kentucky, United States
• Study site — Detroit, Michigan, United States
• Study site — Camden, New Jersey, United States
• Study site — Charlotte, North Carolina, United States
• Study site — Winston-Salem, North Carolina, United States
• Study site — Youngstown, Ohio, United States
• Study site — Midwest City, Oklahoma, United States
• Study site — Medford, Oregon, United States
• Study site — Portland, Oregon, United States
• Study site — Abington, Pennsylvania, United States
• Study site — Hershey, Pennsylvania, United States
• Study site — Johnson, Pennsylvania, United States
• Study site — Pittsburgh, Pennsylvania, United States
• Study site — Kingsport, Tennessee, United States
• Study site — Dallas, Texas, United States
• Study site — Wichita Falls, Texas, United States
• Study site — Payson, Utah, United States

Full record on ClinicalTrials.gov

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