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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02924844
Other study ID # IRB 14/05.03
Secondary ID
Status Completed
Phase N/A
First received October 4, 2016
Last updated October 4, 2016
Start date January 2013
Est. completion date June 2015

Study information

Verified date October 2016
Source Centre Hospitalier Universitaire de Nimes
Contact n/a
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertés
Study type Observational

Clinical Trial Summary

The aim of this before-after study was to assess the impact of a clinical pharmacy bundle of care activities on patient outcomes (length of hospital stay as a primary endpoint) and cost expenditure in two French ICUs.


Recruitment information / eligibility

Status Completed
Enrollment 2787
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Intensive Care Unit patients on weekdays

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nimes

Outcome

Type Measure Description Time frame Safety issue
Other The rate of isolation of multidrug resistant organisms End of hospital stay (expected average of 20 days) No
Primary Length of hospital stay expected average of 20 days No
Secondary Intensive Care Unit length of stay Expected maximum of 10 days No
Secondary Mechanical ventilation duration Expected maximum of 10 days No
Secondary Intensive care unit mortality rate Expected maximum of 10 days No
Secondary Hospital mortality rate End of hospital stay (expected average of 20 days) No
Secondary Patient cost expenditure End of hospital stay (expected average of 20 days) No
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