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Comprison of gnathion-cricoid cartilage distance-based method and weight-based method in determining the size of laryngeal mask airway for adults undergoing ophthalmic surgery: A single center, prospective, randomized, controlled Study.

Comprison of gnathion-cricoid cartilage distance-based method and weight-based method in determining the size of laryngeal mask airway for adults undergoing ophthalmic surgery: A single center, prospective, randomized, controlled Study.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17012689
Enrollment
Unknown
Registered
2017-09-17
Start date
2017-09-01
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

the criteria for laryngeal mask airway selection

Interventions

Weight group(W group):size 4 for those weighting between 50 to 70kg, size 5 for those weighting =70kg
Gnathion-cricoid cartilage distance group(G-C group):size 4 for those G-C distance<11.20cm, size 5 those G-C distance=11.20cm

Sponsors

Zhongshan Ophthalmic Center, Sun Yat-sun University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Patients who will undertake selective ophthalmic surgery; 2. Meet the standard of American Society of Anesthesiologists'(ASA) physical status 1 to 2; 3. Aged 18 to 60 years; 4. Those weighing=50kg and having body mass index (BMI)=30kg/m2; 5. Those with a prediction of less than 2 hour operation time.

Exclusion criteria

Exclusion criteria: 1. having a high risk of regurgitation or aspiration (hiatal hernia, Zenker diverticulum, history of gastro-esophageal reflux disease [GERD],etc); 2. those with a potentially difficult airway (a history of difficulty airway, mouth opening <2 cm, Mallampati class 4, limited neck extension or cervical spine pathology); 3. respiratory tract pathology; 4. with symptomatic acute upper respiratory infection(eg, preoperative sore throat, cough and expectoration,etc); 5. suffered from cardiopulmonary dysfunctions, severe hepatic and renal dysfunctions or conagulation disorder; 6. with loosening or absent of teeth; 7. long-term taking hormore drugs; 8. exiting any other factors that would affect the results of the research.

Design outcomes

Primary

MeasureTime frame
Oropharyngeal leak pressure;

Secondary

MeasureTime frame
????????(%);insertion attempts;tidal volume;Time required for insertion;LMA adjustment required time(s) during the surgery;Ease of airway device placement;Fiberoptic score;Adverse event of laryngopharyngeal after the surgery;

Countries

China

Contacts

Public ContactChen Hongbin

Zhongshan Ophthalmic Center, Sun Yat-sun University

lzr1521@126.com+86 13798000321

Outcome results

None listed

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