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Templates as Cognitive Aids in Emergency Airway Equipment Preparation: the Template Airway Trial

Evaluation and Comparison of Cognitive Aids in Emergency Airway Equipment Preparation: the Randomized, Controlled Template Airway Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06400693
Acronym
TemplateAirway
Enrollment
42
Registered
2024-05-06
Start date
2024-04-15
Completion date
2024-07-23
Last updated
2025-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Airway Management

Brief summary

Comparison of preparation times (in seconds) for emergency airway management (equipment only) with and without a template.

Detailed description

Comparison of time (in seconds) needed to prepare all necessary equipment for one form of emergency airway management with and without a template. Participants will be randomized to preparation with template (A) and preparation without template (B) and all participants will be measured twice for both arms A and B, however, evaluation will take place on two separate days. Methods of airway management evaluated will be endotracheal intubation, supraglottic airway device and oral fiberoptic intubation, with a total of three measurements per participant per study day and two study days per participant. Participants will be nurses in the intensive care unit and, as a control group, anesthesia nurses will also be evaluated in order to factor in the effects of experience. The study will take place in the usual work environment of participants and with the standard equipment.

Interventions

OTHEREndotracheal Intubation

Preparation of all necessary equipment for endotracheal intubation

OTHERSupraglottic Airway

Preparation of all necessary equipment for laryngeal mask

Sponsors

Johannes Gutenberg University Mainz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

single-center, randomized, controlled simulation study

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
Yes

Inclusion criteria

* age 18 years and older * written informed consent * Qualification as a nurse (ICU or anesthesia) * employed with University Medical Centre of Johannes Gutenberg University (JGU) Mainz

Exclusion criteria

* none

Design outcomes

Primary

MeasureTime frameDescription
Time (in seconds) until completion of preparation of necessary equipment for endotracheal intubation between both groupsDefined verbal sign of participant when given task is started and endedComparison of time (in seconds) until completion of preparation of necessary equipment for endotracheal intubation with and without template

Secondary

MeasureTime frameDescription
Time (in seconds) until completion of preparation of necessary equipment for supraglottic airway device between both groupsDefined verbal sign of participant when given task is started and endedComparison of time (in seconds) until completion of preparation of necessary equipment for supraglottic airway device with and without template
Number of missing equipment for endotracheal intubationimmediately after completion of interventionComparison of number of missing equipment for endotracheal intubation with and without template
Number of missing equipment for supraglottic airway between groupsimmediately after completion of interventionComparison of missing equipment for supraglottic airway with and without template
Number of wrong size/equipment between groupsimmediately after completion of interventionComparison of number of wrong size/equipment with and without template
Nasa Task Load Indeximmediately after completion of all 3 assigned interventions on each study dayComparison of work load using Nasa Task Load Index questionnaire with and without template

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026