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The multicenter study of Blockbuster laryngeal mask size selection and performance evaluation

The multicenter study of Blockbuster laryngeal mask size selection and performance evaluation

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-16009105
Enrollment
Unknown
Registered
2016-08-27
Start date
2016-08-29
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

The use of laryngeal mask

Interventions

Blockbuster laryngeal mask group:Blockbuster laryngeal mask
Supreme laryngeal mask group:Supreme laryngeal mask

Sponsors

Friendship Hospital,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Undergo elective surgery under general anesthesia; 2. Aged 18 to 65 years old; 3. Weight 30-100 kg 4. ASA physical status I-II; 5. Understand and write informed patient consent before this study.

Exclusion criteria

Exclusion criteria: 1. Interincisor Distance which is difficult to insert laryngeal masks; 2. The factors which can increase gastric contents regurgitation and respiratory aspiration for the patients; 3. laryngeal lesions; 4. other contraindication about laryngeal mask; 5. lateral position or prone position during operation; 6. predicted difficult airway.

Design outcomes

Primary

MeasureTime frame
time;success rate;grading;pressures;Complication;height;weight;

Secondary

MeasureTime frame
Interincisor Distance;

Countries

China

Contacts

Public ContactTian Ming

Beijing Friendship Hospital, Capital Medical University

13601167650@136.com+86 010-63138362

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026