Intubation using VieScope, video laryngoscopes and conventional laryngoscopy in simulated severe hemorrhage in the airways - a randomized, controlled model study

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00023412

Enrollment

Registered

2021-03-26

Start date

2021-03-19

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

difficult airway

Interventions

Group 1: endotracheal intubation with VieScope Group 2: endotracheal intubation with Videolaryngoscopy (Glidescope) Group 3: endotracheal intubation with conventional endotracheal Intubation (Macintos

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: • male or female volunteers • medical healthcare professionals • Age between 18 and 65 years • Prior written consent following written and verbal information from an investigator

Exclusion criteria

Exclusion criteria: • Persons incapable of giving consent • Age under 18, age over 65 • Rejection of the test subjects • Pregnancy, breastfeeding

Design outcomes

Primary

Measure	Time frame
1. Tube position: tracheal, bronchial, oesophageal (primary endpoint), immediately after Intubation, validated by insufflation of the test lung	—

Secondary

Measure	Time frame
2. Correct tube position for the first intubation - "first pass" (secondary endpoint) 3. Time to Intubation (Secondary Endpoint) 4. Time to first ventilation (secondary endpoint)	—

Countries

Germany

Contacts

Public ContactHannes Ecker

Uniklinik Köln - Klinik für Anästhesiologie und Operative Intensivmedizin

hannes.ecker@uk-koeln.de01703805894

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026