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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03319381
Other study ID # USZ-TRA-SPRKA001
Secondary ID
Status Completed
Phase N/A
First received October 17, 2017
Last updated October 23, 2017
Start date January 1, 2000
Est. completion date December 31, 2012

Study information

Verified date October 2017
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

This study investigated whether there were improvements in the in-hospital mortality, infection rate, and rate of palliative care among geriatric trauma patients after the implementation of new standard operating procedures (SOPs) for the resuscitation room. These new SOPs, comprising early whole-body computed tomography (CT), damage control surgery, and the use of goal-directed coagulation management, were designed for severely injured adult trauma patients


Description:

This study involved the analysis of a prospective single-centre database. Patients admitted via the resuscitation room with need for intensive care treatment after the resuscitation room phase were included and compared before the implementation of the new SOPs (between 1 January, 2000 and 31 December, 2006) and after their implementation in 2009 (between 1 January, 2010 and 31 December, 2012) of our level-I trauma centre.


Recruitment information / eligibility

Status Completed
Enrollment 311
Est. completion date December 31, 2012
Est. primary completion date December 31, 2012
Accepts healthy volunteers No
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

Inclusion in internal trauma database

Exclusion Criteria:

Comprised age < 65 years, ISS < 9, and transfers from other hospitals.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Following new SOPs
The new SOPs comprised early whole-body CT, damage control surgery, and the use of goal-directed coagulation management and are based on the ATLS® concept, which was the strictly followed protocol before implementation of the new SOPs

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Outcome

Type Measure Description Time frame Safety issue
Primary In-hospital mortality In-hospital mortality 30 days
Secondary Infections Infections 30 days
Secondary Rate of palliative care Rate of palliative care 30 days
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