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Distance Hands-on Simulation Training versus Video Instruction for Flexible Laryngeal Mask Airway Management: A Protocol of a Patient-Based, Rater-Blinded, Parallel Group, Randomized Controlled Trial

Distance Hands-on Simulation Training versus Video Instruction for Flexible Laryngeal Mask Airway Management: A Protocol of a Patient-Based, Rater-Blinded, Parallel Group, Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600121867
Enrollment
Unknown
Registered
2026-04-06
Start date
2026-04-06
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

None

Interventions

Remote Training Group:Distance hands-on training
Video Teaching Group:Video instruction
Remote training patient group:Receive general anesthesia with a flexible laryngeal mask
Video-based teaching patient group:Receive general anesthesia with a flexible laryngeal mask

Sponsors

Eye & ENT Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Physician study participants: 1. Clinical physicians with medical licenses; 2. Have conducted no more than 2 cases of flexible laryngeal mask airway management in the past; 3. Agree to participate in the study and sign the informed consent form. Patient study participants: 1. Age 18–65 years old; 2. ASA classification I–II; 3. Scheduled for elective surgery and planned to use flexible laryngeal mask for anesthesia; 4. Agreed to participate in the study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: Physician study participants: 1. Have previously attended laryngeal mask training courses; 2. Have motor dysfunction (such as tremors) that affects hand operation; 3. Lack basic computer skills, making it impossible to complete remote training. Patient study participants: 1. Predicted as having a difficult airway; 2. BMI > 28 kg/m^2; 3. Have other anatomical or pathological factors that affect the safety of laryngeal mask use (such as gastroesophageal reflux).

Design outcomes

Primary

MeasureTime frame
Overall rating scale score;

Secondary

MeasureTime frame
First attempt success rate;Total success rate;Operation time;Modified Brimacombe score;Ventilation parameters;Complications;Learning effect;Training completion and participant satisfaction;

Countries

China

Contacts

Public ContactLi Wenxian/Han Yuan/Wei Wei

Eye & ENT Hospital of Fudan University

liwenxian@eentanesthesia.com+86 21 6437 7134

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026