FOI 2.0 – Impact of Virtual Reality Simulator Training on Awake Fiberoptic Intubation Performance: A Randomized Controlled Trial

FOI 2.0 – Impact of Virtual Reality Simulator Training on Awake Fiberoptic Intubation Performance: A Randomized Controlled Trial - FOI 2.0

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00040728

Enrollment

100

Registered

2026-06-23

Start date

2026-06-29

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Difficult Airway Management: Awake Fiberoptic Intubation

Interventions

Group 1: theory training Group 2: virtuell training

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Members of the Department of Anesthesiology and Intensive Care Medicine - Physicians - Medical students

Exclusion criteria

Exclusion criteria: Refusal to participate

Design outcomes

Primary

Measure	Time frame
- Success rate of fiberoptic intubation (before/after training), including correct tube placement - Time to vocal cord passage (before/after training) - Time to successful airway securement (before/after training) Self-confidence regarding fiberoptic intubation (before/after training) - Perceived benefit of the training - Influence of demographic characteristics (sex and age) and prior experience (medical student/physician status, years of postgraduate training, board certification status, number of previously performed fiberoptic intubations) on the above-mentioned outcome measures	—

Measure

Time frame

- Success rate of fiberoptic intubation (before/after training), including correct tube placement - Time to vocal cord passage (before/after training) - Time to successful airway securement (before/after training) Self-confidence regarding fiberoptic intubation (before/after training) - Perceived benefit of the training - Influence of demographic characteristics (sex and age) and prior experience (medical student/physician status, years of postgraduate training, board certification status, number of previously performed fiberoptic intubations) on the above-mentioned outcome measures

—

Countries

Germany

Contacts

Public ContactJan Wiefhoff

Universitätsklinikum Essen

jan.wiefhoff@uk-essen.de+492017231401

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026