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CompletedNCT02666677INVITEUpdated Apr 4, 2019

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

An observational study in Multiple Trauma, sponsored by Universitätsklinikum Köln. Completed at 1 site in Germany. Per ClinicalTrials.gov, last updated 2019-04-04.

Sponsored by Universitätsklinikum Köln · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
1,500
Sex
All
01

Study summary

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

Read the detailed 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

02

Conditions studied

  • Multiple Trauma

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Keywords

  • polytrauma, emergency medicine
03

In context

Multiple Trauma

131 studies on the registry are indexed under Multiple Trauma; 29 are open to participants now.

This study's enrollment of 1,500 is above the median of 200 across 81 observational studies indexed under Multiple Trauma.

Browse Multiple Trauma studies →

Lead sponsor

Universitätsklinikum Köln is the lead sponsor of 33 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Traumatized patiennts in the emergency department

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients with multiple trauma
  • treated in the emrgency department

Exclusion criteria

Exclusion Criteria:

  • none
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
1,500 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. "Insertion of central venous catheter " survey

    Time frame: Baseline

07

Study locations

1 site
  • University Hospital of Cologne
    Cologne, North Rhine-Westphalia 50937, Germany
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Jan 2016, a primary completion of Dec 2017 and a completion of Dec 2017. It does not say whether these dates are actual or estimated.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 25, 2016
First posted
Jan 28, 2016
Start
Jan 2016
Primary completionActual
Dec 2017
CompletionActual
Dec 2017
Last update
Apr 4, 2019
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 4, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02666677
Lead sponsor
Universitätsklinikum Köln
Collaborators
Universitätsklinikum Leipzig, Wuerzburg University Hospital
Responsible party
Sponsor
First posted
Jan 28, 2016
Start date
Jan 2016
Primary completion
Dec 2017
Completion
Dec 2017
Last update
Apr 4, 2019

Study contacts

Jochen Hinkelbein, MD
principal investigator · UK Köln

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Universitätsklinikum Köln

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