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Pilot study of the additional effect of cadaver training in video laryngoscope intubation education for first-year postgraduate residents

Additional effect of pretreated formalin-fixed cadaver training in video laryngoscope intubation education for first-year postgraduate residents: a single-center randomized parallel-group pilot trial with patient-imagined self-efficacy as the primary outcome - Cadaver-Added Education Trial for Video Laryngoscopy: Pilot Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061035
Enrollment
12
Registered
2026-03-25
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Healthy volunteers (first-year postgraduate residents)

Interventions

Control group Standard mannequin-based video laryngoscope intubation training using the McGRATH video laryngoscope. Each participant will perform 2 intubation attempts on a mannequin. Interventio

Sponsors

Niigata University Medical and Dental Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: First-year postgraduate residents (PGY1) undergoing clinical training at the study institution during the study year Participants with no prior clinical experience in tracheal intubation, or no prior clinical experience in video laryngoscope intubation Written informed consent obtained based on free will after study explanation

Exclusion criteria

Exclusion criteria: Participants unable to attend the training session because of poor physical condition or other reasons Pregnant participants Participants judged inappropriate by the principal investigator for safety or operational reasons

Design outcomes

Primary

MeasureTime frame
Change in patient-imagined self-efficacy for video laryngoscope intubation. The question is: "How confident are you in performing video laryngoscope (McGRATH) intubation under the supervision of an attending physician in an actual patient setting?" A 1-10 numeric rating scale will be used. The change score will be calculated as T1-T0 in the control group and T2-T0 in the intervention group, and compared between groups.

Countries

Japan

Contacts

Public ContactMasataka Hiruma

Niigata University Medical and Dental Hospital Department of Anesthesiology and Intensive Care Unit

m06a066a.med@niigata-u.ac.jp025-227-2338

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026