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Study on a rapid glottic exposure device for remote control tracheal intubation

Study on a rapid glottic exposure device for remote control tracheal intubation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035931
Enrollment
Unknown
Registered
2020-08-20
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-24

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

Conditions

Endotracheal intubation

Interventions

Experimental group:glottic exposure device
control group:traditional method

Sponsors

the Third Affiliated Hospital of the Second Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who need single lumen endotracheal intubation; 2. Patients undergoing general anesthesia; 3. Patients aged 18-65 years; 4. Patients weighing 50-70kg.

Exclusion criteria

Exclusion criteria: 1. Patients who need double lumen endotracheal intubation; 2. Patients with acute respiratory failure; 3. Patients with cardiopulmonary insufficiency; 4. Patients with oral and pharyngeal malformations; 5. Patients with lesions in oral cavity and throat; 6. Patients with loose teeth.

Design outcomes

Primary

MeasureTime frame
time;First time success rate;—

Countries

China

Contacts

Public ContactTao Xiandong

The Third Affiliated Hospital of the Third Medical University

taoxiandong@126.com+86 15802102301

Outcome results

None listed

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