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Ventricular Shunt and Drain Infections - Timing of Reimplantation

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ClinicalTrials.gov Identifier: NCT00470132
Recruitment Status : Completed
First Posted : May 7, 2007
Last Update Posted : August 24, 2012
Sponsor:
Information provided by (Responsible Party):

Study Description
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.

Condition or disease
Ventricular Shunt Infection

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.

Study Design

Study Type : Observational
Actual Enrollment : 400 participants
Observational Model: Cohort
Time Perspective: Retrospective
Official Title: Ventricular Shunt and Drain Infections - Timing of Reimplantation
Study Start Date : May 2007
Primary Completion Date : December 2011
Study Completion Date : December 2011
Groups and Cohorts


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
infected ventricular shunt
Criteria

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.

Exclusion Criteria:

  • Those patients records that do not meet entry criteria
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00470132


Locations
United States, Pennsylvania
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States, 15213
Sponsors and Collaborators
University of Pittsburgh
Investigators
Principal Investigator: Karin Byers, MD University of PIttsburgh and UPMC
More Information

Responsible Party: University of Pittsburgh
ClinicalTrials.gov Identifier: NCT00470132     History of Changes
Other Study ID Numbers: PRO07040262
First Posted: May 7, 2007    Key Record Dates
Last Update Posted: August 24, 2012
Last Verified: August 2012

Keywords provided by University of Pittsburgh:
ventricular shunt

Additional relevant MeSH terms:
Infection
Communicable Diseases