MedPath

Ventricular Shunt and Drain Infections - Timing of Reimplantation

Completed
Conditions
Ventricular Shunt Infection
Registration Number
NCT00470132
Lead Sponsor
University of Pittsburgh
Brief Summary

The retrospective study will help determine whether or not placement of new devices prior to the recommended time was associated with a high risk of relapse or treatment failure.

Detailed Description

The following information will be collected from the medical record retrospectively: demographic data (age, gender, ethnicity, height, weight), past medical history, laboratory results, microbiologic data, data on the patients' devices (type of device, data that it was placed, exchanged or removed), treatment and clinical and microbiological outcomes. This will all be collected retrospectively.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
400
Inclusion Criteria
  • Patients that were cared for by the PI for the purpose of treating an infected ventricular shunt or drainage device for the central nervous system.
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Exclusion Criteria
  • Those patients records that do not meet entry criteria
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Pittsburgh Medical Center

🇺🇸

Pittsburgh, Pennsylvania, United States

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