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Feasibility study of a new method of laryngeal mask placement

Feasibility study of a new method of laryngeal mask placement

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083546
Enrollment
Unknown
Registered
2024-04-28
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Patients requiring auxiliary ventilation

Interventions

Standard method group:The standard placement method is adopted. Standard method: The operator stands at the side of the patients head so that the patients head is in the flower sniffing position, then
New method group:The new placement method is adopted. The operator stands on the opposite side of the patient, first puts the pouch of the laryngeal mask into the patients mouth, then puts the right h

Sponsors

the first hospital of China medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Breast surgery, urology, gynecology patients, age 18-80 years, ASA score 1-3, BMI<30, were eligible for short general anesthesia. Cooperate with experimenters; Participated voluntarily and signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) a difficult airway is known or predicted; (2) Recent sore throat; (3) The opening is less than 2.5 cm; (4) Patients with incorrect exposure risk (non-fasting or gastroesophageal reflux disease); (5) Throat lesions; (6) Patients with trachea compression and tracheomalacia;

Design outcomes

Primary

MeasureTime frame
Whether there was blood when the laryngeal mask was removed;Bronchoscopy to check whether alignment is good and whether adjustment is needed;Whether resistance was encountered during intubation;

Secondary

MeasureTime frame
Heart Rate;mean blood pressure;Insertion time: is the time from picking up the device to connecting it to the respiratory system after the airbag is inflated and confirming that it is in good position;Whether the patient had a sore throat 24 hours after surgery;

Countries

China

Contacts

Public ContactYan Dong

the first hospital of China medical university

m15940271890@163.com+86 159 4027 1890

Outcome results

None listed

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