Viewing Study NCT01963000



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Study NCT ID: NCT01963000
Status: COMPLETED
Last Update Posted: 2013-10-16
First Post: 2013-10-10

Brief Title: Standardized Emergency Care for Community Acquired Pneumonia CAP
Sponsor: Klinikum Nürnberg
Organization: Klinikum Nürnberg

Study Overview

Official Title: Reduction of Mortality in Community-Acquired Pneumonia After Implementing Standardized Care Bundles in the Emergency Department
Status: COMPLETED
Status Verified Date: 2013-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Community acquired pneumonia CAP is associated with a high in-hospital mortality Standardization of diagnostics and adherence to sepsis bundles in the emergency department ED are associated with reduced mortality in patients with sepsis Investigators examined whether the introduction of standardized care bundles and check lists in the ED are associated with a reduced mortality rate in patients hospitalized for CAP

This is an observational trial The investigators retrospectively analyzed performance indicators of 2819 consecutive patients with CAP admitted to the Nuremberg Hospital Germany from 2008 to 2009 At the turn of the year implementation of CAP care bundles took place including interprofessional education checklists and institutionalized feedback Primary endpoint was in-hospital mortality of CAP patients After the implementation of CAP care bundles in the ED mortality of affected patients was significantly lower in 2009 compared to 2008 This study should demonstrate that the implementation of a standardized CAP care bundle in the ED is associated with a risk reduction in affected patients Standardization of diagnostic and therapeutic processes in the ED therefore improves the outcome of patients hospitalized for CAP
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None