Clinical Trials Directory

Trials / Completed

CompletedNCT02044718

Medical Record Study on Adverse Events Requiring a Higher Level of Care in Flemish Hospitals

Status
Completed
Phase
Study type
Observational
Enrollment
878 (actual)
Sponsor
Hasselt University · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

An adverse event (AE) is defined as unintended injury or complication, which results in disability, death or prolongation of hospital stay, and is caused by healthcare management (including omissions) rather than the patient's disease. Retrospective record reviews in several countries have shown that 2,9% to 16,6% of patients in acute hospitals experience one or more AEs. A patient with an AE may require a higher level of care. Although all AEs are important, preventable AEs that result in an upgraded level of patient care are of particular concern. In this study it's defined as an unplanned admission to intensive care unit (ICU) or a Mobile Emergency Team (MET) intervention. The objectives of this study are to determine the incidence of (preventable) adverse events requiring ICU admission or MET intervention and to assess the level of harm of each AE.

Conditions

Timeline

Start date
2011-11-01
Primary completion
2013-06-01
Completion
2013-06-01
First posted
2014-01-24
Last updated
2014-01-24

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02044718. Inclusion in this directory is not an endorsement.