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NCT00235664 · ClinicalTrials.gov registry record

Prospective Study of Drug Resistant Pathogens Among Liver, Intestinal and Multivisceral Transplant Recipients

A clinical trial, sponsored by University of Pittsburgh.

Completed
Registry status
200
Enrollment target

NCT00235664: Completed study, sponsored by University of Pittsburgh.

NCT00235664 is a clinical trial that has completed, run by University of Pittsburgh. The registered enrollment target is 200 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00235664 has completed, sponsored by University of Pittsburgh.

COMPLETED
Registry status
200 participants
Enrollment target

Study Summary

Infections caused by multidrug resistant bacteria have become more prevalent at many tertiary care and academic centers. These infections are associated with increased morbidity and mortality. The initial empiric antibiotic choice may not be adequate and delay in initiating appropriate therapy is a reason for poorer outcomes. Furthermore, not uncommonly the only therapeutic options available are associated with significant toxicity. This is a particular challenge for solid organ transplant recipients, who are immunosuppressed and have a higher risk of acquiring infections. Exposure to different classes of antibiotics has been linked to development of antibiotic resistance. Determining the risk factors for acquisition of drug-resistant bacteria and the molecular mechanisms by which resistance occurs would allow the development and implementation of strategies to minimize these infections and therefore improve outcomes. We, the researchers at the University of Pittsburgh, aim to collect surveillance cultures on patients undergoing liver, intestinal and multivisceral transplantation in order to determine the prevalence and risk factors for Pseudomonas aeruginosa (P. aeruginosa), extended-spectrum β-lactamases (ESBL)-Klebsiella and methicillin-resistant Staphylococcus aureus (MRSA), as well as determine the molecular mechanisms associated with the development of resistance in P. aeruginosa.

Interventions

  • PROCEDURE Collection of stool and endotracheal aspirate samples

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2005-10
Est. Completion 2007-12
University of Pittsburgh

1,238 total trials

What the finished NCT00235664 record still lists

NCT00235664 is an observational study that tracks outcomes without assigning an intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 1 intervention - of which Collection of stool and endotracheal aspirate samples is the first listed.

NCT00235664 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00235664 about?

NCT00235664 is a clinical study titled "Prospective Study of Drug Resistant Pathogens Among Liver, Intestinal and Multivisceral Transplant Recipients". Infections caused by multidrug resistant bacteria have become more prevalent at many tertiary care and academic centers. These infections are associated with increased morbidity and mortality. The initial empiric antibiotic choice may not be adequate and delay in initiating appropriate therapy is a ...

What is the current status of trial NCT00235664?

This trial is currently completed. The enrollment target is 200 participants. The study started on 2005-10. Estimated completion is 2007-12.

What interventions are being tested in trial NCT00235664?

The interventions under investigation include: Collection of stool and endotracheal aspirate samples (PROCEDURE).

Who is sponsoring clinical trial NCT00235664?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT00235664, the US trial registry maintained by the National Library of Medicine. NCT00235664 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.