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Ventilation effect of different ventilation methods in edentulous patients during induction of general anesthesia

Application of a new nasopharyngeal airway combined with improved ventilation technique in edentulous adult patients during induction of general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062471
Enrollment
Unknown
Registered
2022-08-08
Start date
2022-08-10
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

Difficult Mask Ventilation

Interventions

Nasopharyngeal airway group:New nasopharyngeal airway combined with improved ventilation technique
Mask group:Mask ventilation

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Elective surgery under general anesthesia; 2. Edentulous adult patients; 3. ASA I-III; 4. BMI<25kg/m2; 5. Mallampati I-II.

Exclusion criteria

Exclusion criteria: 1. There are other causes of difficult mask ventilation; 2. Severe cardiopulmonary disease, inadequate oxygen storage; 3. There are contraindications to the use of nasopharyngeal airway.

Design outcomes

Primary

MeasureTime frame
Actual tidal volume of supraglottic ventilation within 1min after induction of general anesthesia;—

Secondary

MeasureTime frame
Success rate of ventilation 3min after induction of anesthesia;Adverse events;—

Countries

China

Contacts

Public ContactLingling Wang

The First Affiliated Hospital of Zhengzhou University

yiming2406@126.com+86 13592408335

Outcome results

None listed

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