10-years Nationwide Alpine Accidents in Austria

January 19, 2018 updated by: Mathias Ströhle, Medical University Innsbruck

A Retrospective 10-years Nationwide Observational Study of Alpine Accidents - Flight Accidents, CPR and AED in Alpine Region, Frostbite Injuries and Lightning Strike

This observational study intends to analyze the characteristic of specific accidents happened in Austrian's mountainous regions. The mechanisms of accidents which are evaluated are lightning accidents, cardiopulmonary resuscitation with or without automated external defibrillator, frostbite injuries, accidents with flying vehicle (e.g. paraglider, hang-glider…).

Study Overview

Detailed Description

The data are collected retrospectively from the database of Austrian alpine police force. These data are analyzed. The information from this database (scene of accident, weather, daytime…) is compared to secondary data collected from the University Hospital of Innsbruck. The comparison of both databases was approved by the Austrian Data Protection Agency. The goal of the study is to give detailed information of circumstances leading to accident and give medical information of the patient's condition and his outcome.

Study Type

Observational

Enrollment (Actual)

500

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Innsbruck, Austria, 6020
        • General and Surgical Critical Care Medicine, Medical University of Innsbruck

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 120 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All Patients in the two databases eligible for the searched injury patterns.

Description

Inclusion Criteria:

  • Person suffering the injury searched for;

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
lightning accident
patients suffered injuries due to lightning strike
General and specific data collected
frostbite
patients suffered injuries due to local hypothermia leading to frostbite injuries
General and specific data collected
cpr and aed
patients suffered cardiac arrest in alpine region treated with or without automated external defibrillatior
General and specific data collected
flight accident
patients suffered injuries due to use of a flying vehicle in mountainous regions.
General and specific data collected

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of persons suffered an accident in Alpine Mountains in Austria
Time Frame: 2005-2015
The number of persons (n/year) which suffered one of the specified accidents.
2005-2015
Gender of persons suffered an accident in Alpine Mountains in Austria
Time Frame: 2005-2015
Gender male/female or non specified which suffered one of the specified accidents.
2005-2015
Mortality of persons suffered an accident in Alpine Mountains in Austria
Time Frame: 2005-2015
Number of persons deceased (deceased/n per year) which suffered one of the specified accidents.
2005-2015

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of pattern like injured patients treated in University Hospital of Innsbruck, a major tertiary trauma center in western Austria.
Time Frame: 2005-2015
(n/year) treated in University Hospital of Innsbruck
2005-2015
Gender of pattern like injured patients treated in University Hospital of Innsbruck, a major tertiary trauma center in western Austria.
Time Frame: 2005-2015
male/female, unspecified treated in University Hospital of Innsbruck
2005-2015
Injury severity score (ISS) of pattern like injured patients treated in University Hospital of Innsbruck, a major tertiary trauma center in western Austria.
Time Frame: 2005-2015
Injury severity score of suffered injury (ISS=AIS*AIS)
2005-2015
Abbreviated Injury severity scale (AIS) of pattern like injured patients treated in University Hospital of Innsbruck, a major tertiary trauma center in western Austria.
Time Frame: 2005-2015
Abreviated Injury severity scale of suffered injury (1-6 points; scale - minor, moderate, serious, severe, critial, maximum)
2005-2015
Type of evacuation and mortality
Time Frame: 2005-2015
Type of evacuation (terrestrial, helicopter, combined terrestrial and helicopter) and the mortality for each group (deceased/n per year)
2005-2015

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Peter Paal, Dr, Hospital of Barmherzige Brüder Salzburg

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 21, 2015

Primary Completion (Actual)

August 31, 2017

Study Completion (Actual)

August 31, 2017

Study Registration Dates

First Submitted

November 28, 2017

First Submitted That Met QC Criteria

January 19, 2018

First Posted (Actual)

January 23, 2018

Study Record Updates

Last Update Posted (Actual)

January 23, 2018

Last Update Submitted That Met QC Criteria

January 19, 2018

Last Verified

January 1, 2018

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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