Clinical Trials Directory

Trials / Completed

CompletedNCT00280904

A Registry for Comparing Catheter-Related Infection Rates Among Various Shunt Systems in the Treatment of Hydrocephalus

Status
Completed
Phase
Study type
Observational
Enrollment
433 (actual)
Sponsor
Codman & Shurtleff · Industry
Sex
All
Age
Healthy volunteers
Not accepted

Summary

The purpose of this Registry is to compare shunt/catheter-related infection rates among various shunt systems when used according to hospital standard of care to treat hydrocephalus.

Detailed description

Clinical trials show that the majority of infections in shunt systems originate from bacterial contamination introduced at the time of surgery and most appear by 3-4 weeks post-operatively. Protection must persist well beyond the surgical procedure to make certain that all contaminating bacteria are completely eradicated. Depending upon the institution, shunt infection rates have been known to be as little as 1% to as much as 25%. However, two prospective trials that have been published from large databases, with a consistent definition of infection, have indicated an overall infection rate of approximately 10% This prospective non-randomized, open-label Registry is designed to investigate and identify short-term shunt/catheter-related infection rates in ventriculoperitoneal shunt systems using various catheters during hospital standard of care treatment of Subjects with hydrocephalus. Prospective Subjects will include those receiving shunts for the first time (de novo) and those with previously implanted shunts for whom catheter or total system replacements are required. This Registry will enroll 450 implanted Subjects of any age who meet all the inclusion criteria and none of the exclusion criteria and who provide signed Informed Consent to participate in this clinical Registry Subjects will be followed for up to 90 days.

Conditions

Interventions

TypeNameDescription
DEVICEShunt catheterstandard of care implantation of shunt (any brand). Subjects are followed for 90 days to obtain information about whether or not an infection occurred.

Timeline

Start date
2006-01-01
Primary completion
2008-04-01
Completion
2008-04-01
First posted
2006-01-24
Last updated
2013-03-08
Results posted
2013-03-08

Locations

8 sites across 6 countries: United States, Canada, China, Hong Kong, India, Singapore

Source: ClinicalTrials.gov record NCT00280904. Inclusion in this directory is not an endorsement.