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Laryngeal mask seal observation study

Laryngeal mask seal observation study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600115979
Enrollment
Unknown
Registered
2026-01-04
Start date
2026-01-19
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

None

Interventions

Observation group:None

Sponsors

Haiyan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18-60 years; ASA class I-II; scheduled for surgery under general anesthesia; provided informed consent.

Exclusion criteria

Exclusion criteria: History of difficult airway; pharyngeal lesions; high risk of gastroesophageal reflux; pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
First-time implantation success rate;Incidence of throat injury;

Secondary

MeasureTime frame
Overall Implantation Success Rate (Within 3 attempts);Placement operation time (from the moment the laryngeal mask leaves the lips to the appearance of the first EtCO2 waveform);Laryngeal mask airway sealing pressure (peak airway pressure at leak);Intraoperative ventilation quality (oxygenation, stability of ventilation parameters);

Countries

China

Contacts

Public ContactQinfeng Sun

Haiyan People's Hospital

jxme@163.com+86 573 8622 3369

Outcome results

None listed

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