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Physician-nurse Team to Reduce Emergency Department (ED) Overcrowding

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01219868
First Posted: October 13, 2010
Last Update Posted: March 20, 2013
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 (Responsible Party):
Olivier T. Rutschmann, University Hospital, Geneva
October 6, 2010
October 13, 2010
March 20, 2013
October 2010
January 2011   (Final data collection date for primary outcome measure)
ED length of stay [ Time Frame: 3 months ]
Same as current
Complete list of historical versions of study NCT01219868 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Physician-nurse Team to Reduce Emergency Department (ED) Overcrowding
Impact of Physician-nurse Team on ED Length of Stay
The objective of this study is to explore the impact of a physician-nurse team supervising patient's flow on ED length of stay
A physician-nurse team will be in charge of patients flow in the ED during intervention periods. During control periods, no team will be present. The impact of this team on Ed length of stay will be assessed.
Interventional
Not Provided
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Triage
Behavioral: Physician-nurse team supervision
Physician-nurse team will supervise patient's flow in the ED
Other Name: No name
Experimental: Physician-nurse team
Intervention: Behavioral: Physician-nurse team supervision
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
8000
March 2011
January 2011   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • all adult patients > 16 years presenting to the ED

Exclusion Criteria:

Sexes Eligible for Study: All
16 Years and older   (Child, Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Switzerland
 
 
NCT01219868
SU-001
No
Not Provided
Not Provided
Olivier T. Rutschmann, University Hospital, Geneva
University Hospital, Geneva
Not Provided
Principal Investigator: Olivier T Rutschmann, MD, MPH HUG
University Hospital, Geneva
March 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP