We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Effects of Isolated Rooms on the Prevalence of Hospital Acquired Pneumonia in a Respiratory ICU

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01250691
First Posted: December 1, 2010
Last Update Posted: December 1, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Eskisehir Osmangazi University
November 30, 2010
December 1, 2010
December 1, 2010
January 2004
July 2008   (Final data collection date for primary outcome measure)
Not Provided
Not Provided
No Changes Posted
Not Provided
Not Provided
Not Provided
Not Provided
 
Effects of Isolated Rooms on the Prevalence of Hospital Acquired Pneumonia in a Respiratory ICU
Epidemiologic Study of Hospital Acquired Pneumonia in a Respiratory ICU
This study will carry out in the ICU. Objectives of the study are to determine the frequency of HAP and the effect of isolated rooms on the frequency of pneumonia in the ICU.
In the present study, it was aimed to determine the incidence, causative agents, antimicrobial resistance, and risk factors for lower respiratory tract infections in patients followed in the ICU for the last 4 years. The effect of reconfiguration from a ward-type ICU consisting one large room to an ICU with isolated rooms with two beds on the incidence of HAP was also determined.
Observational
Observational Model: Cohort
Time Perspective: Cross-Sectional
Not Provided
Not Provided
Non-Probability Sample
All of the patients who had been admitted to the ICU during this period were included in the study
  • Pneumonia
  • Intensive Care Unit
Other: ward-type ICU
frequency of hospital acquired pneumonia in the ICU
Other Name: frequency of hospital acquired pneumonia in the ICU
  • hospital acquired pneumonia
  • isolated rooms
    Intervention: Other: ward-type ICU
  • ward-type ICU
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
532
August 2010
July 2008   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • adult patients,
  • admitted to the ICU

Exclusion Criteria:

  • trauma, surgery or burned patients
  • patients under 18
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Turkey
 
 
NCT01250691
HAP-OU-isolation
Yes
Not Provided
Not Provided
Eskisehir Osmangazi University, Department of Chest Diseases, Intensive Care Unit, Eskisehir Osmangazi University
Eskisehir Osmangazi University
Not Provided
Study Chair: Irfan Ucgun, As.Prof.Dr. Eskisehir Osmangazi University, Medical Faculty
Eskisehir Osmangazi University
January 2004