- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06322134
Drowning Incidents Treated by the Danish SAR Helicopters (DROWN_SAR)
Incidence and Characteristics of Drowning Patients at Sea Treated by the Royal Danish Air Force's Search And Rescue Helicopters From 2014-2023: a Nationwide Registry-based Study
Study Overview
Status
Conditions
- Drowning
- Drowning; Anoxia
- Drowning, Near
- Drowning and Nonfatal Submersion
- Drowning or Immersion of Unknown Intent
- Drowning and Submersion, Undetermined Intent
- Drowning and Submersion While in Natural Water
- Drowning and Submersion Due to Sailboat Sinking
- Drowning and Submersion Due to Fall Off Ship
- Drown
Intervention / Treatment
Detailed Description
The national Danish Drowning Cohort contains data on all fatal and non-fatal drowning patients treated by the Emergency Medical Services. However, data on drowning patients treated by the SAR helicopters is reported in a separate system.
The population of drowning patients treated by the SAR helicopters has never been described, thus contributing to the potential underreporting of the most critically ill drowning patients in Denmark. Given the rarity of drowning, registry-based studies are needed to provide patient characteristics and evaluate critical care interventions performed on this group of patients.
This study aims to identify and describe a national cohort of drowning patients at sea treated by the Royal Danish Air Force's SAR helicopters from 2014 to 2023.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Region Zealand
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Næstved, Region Zealand, Denmark, 4700
- Prehospital Center
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Drowning patients will be identified through manual validation of the Royal Danish Air Force's SAR helicopter's records using the internationally accepted definitions of fatal and non-fatal drowning incidents.
Drowning was defined by the WHO in 2002 as "the process of experiencing respiratory impairment from submersion or immersion in liquid".
If the incident involved submersion or immersion, but the patient did not experience respiratory impairment, the incident was categorised as a water rescue.
Description
Inclusion Criteria:
- Patients treated by the Danish SAR helicopters AND
- Drowning as defined by the WHO (the process of experiencing respiratory impairment from submersion or immersion in liquid)
Exclusion Criteria:
- Patients who have not been immersed or submersed.
- Duplets.
- Interhospital transfers.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Fatal drowning
Prehospital mortality following a drowning incident, defined as a dichotomous variable (dead or alive) evaluated at case termination.
Patients admitted to the hospital with cardiac arrest were considered fatal drowning incidents in this study.
|
Patients categorized as drowning have been experiencing respiratory impairment from submersion or immersion in liquid and needing rescue by the Royal Danish Air Force's Search and Rescue (SAR) helicopters.
|
|
Non-fatal drowning
Drowning incidents where the patient had spontaneous circulation at hospital admission.
|
Patients categorized as drowning have been experiencing respiratory impairment from submersion or immersion in liquid and needing rescue by the Royal Danish Air Force's Search and Rescue (SAR) helicopters.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Annual incidence of drowning treated by the Danish SAR helicopters from 2014-2023
Time Frame: 1 year
|
The incidence will be reported as the annual number of cases.
|
1 year
|
|
Annual incidence rate of drowning treated by the Danish SAR helicopters from 2014-2023
Time Frame: 1 year
|
The incidence rate as the annual number of cases per 100,000 person-years.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Spatial distribution of drowning patients treated by the Danish SAR helicopters from 2014-2023
Time Frame: The map will display all drowning incidents treated by the Danish SAR helicopters from 2014-2023.
|
The spatial distribution of drowning incidents will be displayed on a map of Denmark, with each case presented with a single entry based on the geographical coordinates of the incident.
|
The map will display all drowning incidents treated by the Danish SAR helicopters from 2014-2023.
|
Collaborators and Investigators
Collaborators
Investigators
- Study Director: Helle Collatz Christensen, Ass. Prof., Prehospital Center, Region Zealand
Publications and helpful links
General Publications
- Breindahl N, Wolthers SA, Jensen TW, Holgersen MG, Blomberg SNF, Steinmetz J, Christensen HC; Danish Cardiac Arrest Group. Danish Drowning Formula for identification of out-of-hospital cardiac arrest from drowning. Am J Emerg Med. 2023 Nov;73:55-62. doi: 10.1016/j.ajem.2023.08.024. Epub 2023 Aug 15.
- Breindahl N, Wolthers SA, Moller TP, Blomberg SNF, Steinmetz J, Christensen HC; Danish Drowning Validation Group. Characteristics and critical care interventions in drowning patients treated by the Danish Air Ambulance from 2016 to 2021: a nationwide registry-based study with 30-day follow-up. Scand J Trauma Resusc Emerg Med. 2024 Mar 6;32(1):17. doi: 10.1186/s13049-024-01189-y.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- DROWN_SAR
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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