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NCT01904305 Clinical Trial

Clinician Ability to Predict the Presence of Nosocomial Pneumonia Based on Bronchoscopic Findings

Pneumonia Clinical Trial

Official title:
Clinician Ability to Predict the Presence of Nosocomial Pneumonia Based on Macroscopic Examination of Bronchoscopic Findings in Critically Ill Surgical Patients

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01904305
Other study ID # Robinson-2010-01
Secondary ID
Status Completed
Phase N/A
First received November 18, 2011
Last updated July 17, 2013
Start date January 2011
Est. completion date February 2013

Study information
Verified date July 2013
Source University of Cincinnati
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial Summary

This study aims to determine whether interpretations of bronchoscopic results enable physicians to successfully predict the presence of pneumonia in traumatically injured patients.

Description:

This study aims to determine whether interpretations of bronchoscopic results enable physicians to successfully predict the presence of pneumonia in traumatically injured patients. Bronchoscopies will be videotaped. The clinician doing the procedure will make prediction as to whether the patient, in fact, has pneumonia. In addition, at least one other physician will view the videotape and predict whether the patient has pneumonia.

Once laboratory results are available, the physician predictions will be compared against the definitive laboratory determination

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date February 2013
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Critical Care staff and fellows of the Departments of Anesthesia and Surgery

Exclusion Criteria:

- Refusal of consent

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States University Hospital Cincinnati Ohio

Sponsors (1)
Lead Sponsor Collaborator
University of Cincinnati

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Presence or absence of hospital-acquired pneumonia When pneumonia is suspected, patient with undergo bronchoscopy. BAL specimens will be submitted to laboratory testing. Laboratory results are the definitive indication of pneumonia, or lack thereof. At first clinical suspicion of pneumonia. Average of hospital Day 4 No
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