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Evaluation of clinical application of SaCoVLMTM laryngeal mask in general anesthesia

Evaluation of clinical application of SaCoVLMTM laryngeal mask in general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000028802
Enrollment
Unknown
Registered
2020-01-04
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-01-06

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

Conditions

visual laryngeal mask

Interventions

Case series:visual laryngeal mask

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. ASA grade I, II; 3. BMI 18kg to 30Kg/m2 4. Mallampati grades 1-2.

Exclusion criteria

Exclusion criteria: 1. severe respiratory diseases; 2. The operation position is lateral or prone position; 3. Patients with increased reflux of gastric contents and respiratory aspiration: Including fasting, morbid obesity, more than 14 weeks of pregnancy, frequent gastroesophageal reflux, intestinal obstruction, and hiatal hernia 4. Other laryngeal masks are relatively contraindicated, such as intra-oral throat surgery and chest surgery; 5. Patients known to be allergic to any component of propofol and remifentanil.

Design outcomes

Primary

MeasureTime frame
observe the visible glottis after the laryngeal mask is placed;

Secondary

MeasureTime frame
oral-laryngeal pressure of visual laryngeal mask;successful rate of visual laryngeal mask;the implacement time of visual laryngeal mask;postoperative complication rates;

Countries

China

Contacts

Public ContactZuo Mingzhang

Beijing Hospital

zuomingzhang0792@bjhmoh.cn+86 13911589738

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026