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The clinical effect analysis of SaCoVLM visual laryngeal mask guided intubation and I-gel laryngeal mask combined with visual soft mirror guided intubation in airway management under general anesthesia

The clinical effect analysis of SaCoVLM visual laryngeal mask guided intubation and I-gel laryngeal mask combined with visual soft mirror guided intubation in airway management under general anesthesia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043443
Enrollment
Unknown
Registered
2021-02-18
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

The clinical effect analysis of SaCoVLM visual laryngeal mask guided intubation and I-gel laryngeal mask combined with visual soft mirror guided intubation in airway management under general anesthes

Interventions

SaCoVLM visual laryngeal mask group:SaCoVLM visual laryngeal mask guided intubation after induction of general anesthesia
I-gel laryngeal mask combined with visual soft mirror guided intubation group :After induction of general anesthesia, I-gel laryngeal mask combined with visual soft mirror guided intubation

Sponsors

Peking University Fifth Clinical School (Beijing Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. All patients understand the purpose of this research and sign an informed consent form. 2. Aged >= 18 years, no gender limit. 3. ASA I-II grade. 4. Plan to perform tracheal intubation with elective general anesthesia. 5. Operation time is less than 4 hours.

Exclusion criteria

Exclusion criteria: 1. Person with restricted mouth; 2. Patients with upper respiratory tract tumors, abscesses, foreign bodies or narrow airways; 3. Those who have a history of difficult airway disease; 4. Patients who require one-lung ventilation during thoracic surgery; 5. BMI >= 35.

Design outcomes

Primary

MeasureTime frame
Success rate of tracheal intubation ;

Secondary

MeasureTime frame
Laryngeal mask insertion time ;Number of laryngeal mask insertions;oropharyngeal leak pressure;Endotracheal intubation time;Number of intubations;Classification of glottal exposure under visual soft lens;Postoperative sore throat, bleeding, dislocation of dipper cartilage, hoarseness and dysphagia;SBP, DBP, MAP, HR, SpO2;

Countries

China

Contacts

Public ContactZuo Mingzhang

Peking University Fifth Clinical School (Beijing Hospital)

zuomingzhang0792@bjhmoh.cn+86 13911589738

Outcome results

None listed

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