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Completed No phase listed Observational

Normal Pressure Hydrocephalus (NPH) Registry

ClinicalTrials.gov ID: NCT00233701

Public ClinicalTrials.gov record NCT00233701. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 10:35 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00233701
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Codman & Shurtleff
Industry
Enrollment
343 participants

Conditions and interventions

Interventions

Not listed

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2004 (Type not available)
Primary completion
Sep 2008 (Actual)
Completion
Sep 2008 (Actual)
Last update posted
Feb 8, 2010

2004 – 2008

United States locations

U.S. sites
28
U.S. states
21
U.S. cities
28
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Los Angeles California — —
Not listed Boulder Colorado — —
Not listed Jacksonville Florida — —
Not listed Macon Georgia — —
Not listed Boise Idaho — —
Not listed Chicago Illinois — —
Not listed Iowa City Iowa — —
Not listed Lexington Kentucky — —
Not listed Detroit Michigan — —
Not listed Camden New Jersey — —
Not listed Charlotte North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Youngstown Ohio — —
Not listed Midwest City Oklahoma — —
Not listed Medford Oregon — —
Not listed Portland Oregon — —
Not listed Abington Pennsylvania — —
Not listed Hershey Pennsylvania 17033 —
Not listed Johnson Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed Kingsport Tennessee — —
Not listed Dallas Texas — —
Not listed Wichita Falls Texas — —
Not listed Payson Utah — —
Not listed Salt Lake City Utah — —
Not listed Richmond Virginia 23298-0449 —
Not listed La Crosse Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00233701, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 8, 2010 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00233701 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →