FindTrial
Sign In

Evaluation of a Newly Developed Respiratory Volume Monitoring Equipment: A Simulation-Based Study

Evaluation of user suitability of respiratory volume monitoring equipment for emergency medical technicians

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011169
Enrollment
20
Registered
2025-11-17
Start date
2023-09-18
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

None listed

Interventions

None listed

Sponsors

Yonsei University Wonju College of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Emergency medical technicians or paramedics who use manual ventilation. ? Those who can understand and follow the training and instructions provided in this study. ? Those who can apply an endotracheal tube to a patient (mannequin).

Exclusion criteria

Exclusion criteria: ? Subjects who did not meet the selection criteria were excluded from this study ? Subjects deemed unsuitable by the research director or other staff

Design outcomes

Primary

MeasureTime frame
User Satisfaction Survey (Normal Scenario - Ambubagging)—

Secondary

MeasureTime frame
User Satisfaction Survey (Intubation Scenario - ET-tube);User Satisfaction Survey (Intubation Scenario - I-gel Tube);Ease of Use, Identification & Understandability Survey ( Normal Scenario - Ambubagging);Ease of Use, Identification & Understandability Survey (Intubation Scenario - ET-tube);Ease of Use, Identification & Understandability Survey (Intubation Scenario - I-gel Tube);Subjective feedback on strengths, weaknesses, and areas for improvement—

Countries

Korea, Republic of

Contacts

Public ContactHee Young Lee

Yonsei University Wonju College of Medicine

hylee3971@yonsei.ac.kr+82-33-741-0952

Outcome results

None listed

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