Effects of best evidence practice of airwaymanagement training in HEMS

Phase 3

• Conditions: - neurological deficit with risk of aspiration, unconsciousness- Severe trauma with: RRsys <90mmHg, hypoxia <90% SpO2, SHT GCS <9- necessary airway protection for air transport- cardiopulmonary resuscitation; R57.1; J96.0; S06.7; I46.9; Hypovolaemic shock; Acute respiratory failure; Intracranial injury with prolonged coma; Cardiac arrest, unspecified

• Registration Number: DRKS00023889
• Lead Sponsor: Kliniken der Stadt KölnKrankenhaus Köln MerheimLuftrettungszentrum Christoph 3

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-04-01
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Patients in the context of preclinical emergency medical treatment
- Preclinical indications for securing the airway by endotracheal intubation (neurological deficit with risk of aspiration, unconsciousness, severe trauma with: RRsys <90mmHg, hypoxia <90% SpO2, SHT GCS <9, necessary airway securing for air transport, cardiopulmonary resuscitation)
- Patients over the age of 18
- Fulfill all criteria for using the video laryngoscope or Bougie according to the manufacturer's instructions
- If the condition of the patient allows, appropriate oral information

Exclusion Criteria

- Failure to meet an inclusion criterion
- Opting of the treating emergency doctor for another method of airway management
- Any other condition which, in the opinion of the investigator, makes the subject appear unsuitable for inclusion in the study.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
First pass success of preclinical intubation,<br>Duration until successful airway measurement

Secondary Outcome Measures

Name	Time	Method
Correlation of the real preclinical parameters with the parameters of the body course