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NCT02666677 Clinical Trial

INVITE Study: Invasive Instrumentation in Trauma Patients in the Shock Room

Multiple Trauma Clinical Trial

— INVITE  

Official title:
Invasive Instrumentation in Trauma Patients in the Shock Room: A Online-survey for Anaesthesia Departments in Germany

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02666677
Other study ID # INVITE
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2016
Est. completion date December 2017

Study information
Verified date April 2019
Source Universitätsklinikum Köln
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is an online survey asking for invasive instrumention in trauma patients of an emergency department

Description:

The INVITE study is an online survey for medical doctors asking for invasive instrumention (e.g., arterial line, entral venous line, etc.) in trauma patients of an emergency department

Recruitment information / eligibility
Status Completed
Enrollment 1500
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with multiple trauma

- treated in the emrgency department

Exclusion Criteria:

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Germany University Hospital of Cologne Cologne NRW

Sponsors (3)
Lead Sponsor Collaborator
Universitätsklinikum Köln Universitätsklinikum Leipzig, Wuerzburg University Hospital

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary "Insertion of central venous catheter " survey Baseline
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