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RecruitingNCT06310486DROWN_CALLUpdated Jun 4, 2025

The Emergency Call on Drowning

An observational study in Drowning, Drowning; Anoxia and Drowning, Near, sponsored by Prehospital Center, Region Zealand. Recruiting at 1 site in Denmark. Per ClinicalTrials.gov, last updated 2025-06-04.

Sponsored by Prehospital Center, Region Zealand · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
  • Started Jan 2016; still recruiting 10 years 10 months later.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
1,500
Sex
All
01

Study summary

This study aims to 1) describe patient-, setting-, and dispatcher-related characteristics in drowning-related emergency calls to the Emergency Medical Dispatch Centre (1-1-2 emergency phone) and 2) factors associated with 30-day survival. The investigators will separately analyse drowning-related out-of-hospital cardiac arrest (OHCA) and drowning-related non-OHCA. If feasible, the investigators will qualitatively analyse the calls to identify and describe potential barriers for an optimal handling strategy.

Read the detailed description

Previous studies have explored emergency priority levels, emergency call categorisations, barriers to assessing an emergency call, and the effects on the outcome. However, this has never been done specifically for drowning patients. Drowning presents a rare and special circumstance that may be particularly complex for laypeople and medical dispatchers for several reasons. Despite this complexity and medical dispatchers' potential to optimize treatment and improve outcomes in drowning incidents, the characteristics of drowning-related emergency calls have never been explored.

This protocol presents a registry-based cohort study of drowning-related emergency medical calls to the EMDC (1-1-2 emergency phone) with 30-day follow-up.

Data from the national Danish Prehospital Drowning Data will be linked with audio files and electronic data from the EMDC database using the patient's unique civil registration numbers.

The investigators will construct two lists of variables: one list for OHCA and one for non-OHCA emergency calls. Data collection from the EMDC database will consist of three phases.

In phase 1, three independent reviewers will listen to 20 emergency calls on drowning (10 OHCA and 10 non-OHCA) to identify relevant variables from the calls (e.g., presence of key symptoms [since an emergency call often does not contain information regarding the absence of symptoms], communication barriers [anything that comes in the way of receiving and understanding information], pre-arrival instructions to callers etc.).

In phase 2, the same reviewers will listen to 20 other emergency calls (10 OHCA and 10 non-OHCA) and use the lists for data collection to determine the data availability and completeness. This may result in modifications to the lists of variables. The investigators will use the results as a basis for reviewer training and calculate inter-rater reliability.

Once the reviewers' performances are satisfying (defined as Fleiss kappa ≥0.8), the investigators will move to phase 3 and collect data for all the drowning calls. Emergency calls will be stratified as OHCA or non-OHCA calls.

02

Conditions studied

  • Drowning
  • Drowning; Anoxia
  • Drowning, Near
  • Drowning; Asphyxia
  • Drowning and Nonfatal Submersion
  • Drowning or Immersion of Unknown Intent
  • Drowning and Submersion, Undetermined Intent
  • Drowning and Submersion While in Bath-Tub
  • Drowning and Submersion While in Natural Water
  • Drowning and Submersion Due to Sailboat Sinking
  • Drowning and Submersion Due to Fall Off Ship
  • Drowning and Submersion While in Swimming-Pool

Keywords

  • Emergency Medical Service (EMS)
  • Drowning
  • Emergency Medical Dispatch Centre
  • Emergency Medical Coordination Centre
  • Dispatch
  • Emergency Call
  • Registry
  • Database
  • Epidemiology
  • Danish Drowning Formula
  • Danish Prehospital Drowning Data
  • Utstein
03

In context

Drowning

21 studies on the registry are indexed under Drowning; 6 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 1,099 across 14 observational studies indexed under Drowning.

Browse Drowning studies →

Lead sponsor

Prehospital Center, Region Zealand is the lead sponsor of 16 studies on the registry; 4 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

All validated drowning cases registered in the Danish Prehospital Drowning Data will be linked with data from the EMDC database according to a data minimisation principle. Patients are included in the Danish Prehospital Drowning Data if they have experienced a drowning incident between 2016 and 2023, defined as experiencing respiratory impairment from submersion or immersion in liquid.

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 at all ages registered in the Danish Prehospital Drowning Data are eligible.

Exclusion criteria

Exclusion Criteria:

  • Obvious clinical signs of irreversible death (decapitation, decomposition, post-mortem lividity, post-mortem rigidity)
  • A valid Do-Not-Attempt-Resuscitation (DNAR) order or other code status orders limiting life-sustaining therapies
  • Missing or corrupted audio files
  • Missing identification number
  • Missing 30-day survival
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
1,500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Fatal drowning

    These patients experienced a drowning incident and died within 30 days after the incident because of their submersion injury.

    Other: Drowning-related OHCA · Other: Drowning-related non-OHCA

  • Non-fatal drowning

    These patients experienced a drowning incident and survived until 30 days after the incident.

    Other: Drowning-related OHCA · Other: Drowning-related non-OHCA

Interventions

  • OtherDrowning-related OHCA

    These patients were involved in a drowning incident (submersion or immersion in liquid) and experienced out-of-hospital cardiac arrest (OHCA), defined as being unconscious and not breathing normally at any time in the prehospital setting. Some of these patients may die as a consequence of the submersion injury (fatal drowning), while others may survive (non-fatal drowning).

  • OtherDrowning-related non-OHCA

    These patients were involved in a drowning incident (submersion or immersion in liquid) but did not experience an OHCA. Some of these patients may die as a consequence of the submersion injury (fatal drowning), while others may survive (non-fatal drowning).

06

What researchers measure

Primary outcomes

  1. Patient-related characteristics influencing the 30-day survival

    Describe patient-related characteristics in drowning-related emergency calls to the EMDC (1-1-2 emergency phone)

    Time frame: 30 days after the drowning incident

  2. Setting-related characteristics influencing the 30-day survival

    Describe setting-related characteristics in drowning-related emergency calls to the EMDC (1-1-2 emergency phone)

    Time frame: 30 days after the drowning incident

  3. Caller-related characteristics influencing the 30-day survival

    Describe caller-related characteristics in drowning-related emergency calls to the EMDC (1-1-2 emergency phone)

    Time frame: 30 days after the drowning incident

  4. Dispatcher-related characteristics influencing the 30-day survival

    Describe dispatcher-related characteristics in drowning-related emergency calls to the EMDC (1-1-2 emergency phone)

    Time frame: 30 days after the drowning incident

07

Study locations

1 of 1 sites recruiting
08

References and documents

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. PubMed 37619443 ↗
  • 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. PubMed 38448994 ↗

Individual participant data

Plan to share: No — The datasets used and analysed during the current study are available from the corresponding author upon reasonable request.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2016 (actual). Primary completion is estimated for Dec 2025, 119 months after the start.

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

Registered
Mar 7, 2024
First posted
Mar 15, 2024
StartActual
Jan 1, 2016
Primary completionEst.
Dec 31, 2025
CompletionEst.
Dec 31, 2025
Last update
Jun 4, 2025
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 Jun 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06310486
Lead sponsor
Prehospital Center, Region Zealand
Responsible party
Niklas Breindahl (Principal Investigator, Prehospital Center, Region Zealand) — Principal investigator
First posted
Mar 15, 2024
Start date
Jan 1, 2016
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Jun 4, 2025

Study contacts

Niklas Breindahl, MD, PhD
Contact
niklas.breindahl@gmail.com
+4528566410
Helle Collatz Christensen, MD, PhD, Ass. Prof.
study director · Prehospital Center, Region Zealand

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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