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To compare the clinical effect of SaCoVLM TM visual laryngeal mask guided intubation and UE visual laryngoscope intubation in airway management under general anesthesia

To compare the clinical effect of SaCoVLM TM visual laryngeal mask guided intubation and UE visual laryngoscope intubation in airway management under general anesthesia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070761
Enrollment
Unknown
Registered
2023-04-23
Start date
2023-05-01
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Airway management

Interventions

SaCoVLM group and UE group:SaCoVLM intubation was selected

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Understand the purpose of the study and sign the informed consent 2. Age =18 years old, gender unlimited 3. ASA Grade I-II 4. Scheduled tracheal intubation under general anesthesia 5. The operation time is less than 4 hours 6, 18 kg/m2 = BMI = 35 kg/m2

Exclusion criteria

Exclusion criteria: 1. Mouth opening is limited, and the mouth opening degree is less than 2cm 2. Patients with upper respiratory tract tumors, abscesses, foreign bodies or airway stenosis 3. Patients requiring single lung ventilation in thoracic surgery 4. Head and neck surgery 5. Laryngoscope cannot be inserted into sternomental adhesion 6?BMI 35 kg/m2

Design outcomes

Primary

MeasureTime frame
Success rate of first intubation;Overall success rate of endotracheal intubation;

Secondary

MeasureTime frame
Hemodynamic changes before and after intubation;Intubation time for both devices;Number of intubations;With or without laryngeal compression assistance;Subglottic exposure grading with both devices;Hemodynamic changes before and after removal of the endotracheal tube;Hemodynamic changes before and after removal of the laryngeal mask;Tracheal tube blood staining;Pharyngeal pain 24 h after operation;dysphagia;arytenoid dislocation;Incidence of hoarseness;

Countries

China

Contacts

Public ContactChun-ling Yan

Beijing Hospital

yanchunling19800@sina.com+86 13651364019

Outcome results

None listed

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