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Efficacy and safety of adjustable visual laryngeal mask airway in total hip arthroplasty surgery under lateral decubitus position: a randomized clinical trial

Efficacy and safety of adjustable visual laryngeal mask airway in total hip arthroplasty surgery under lateral decubitus position: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104912
Enrollment
Unknown
Registered
2025-06-25
Start date
2025-07-10
Completion date
Unknown
Last updated
2025-06-30

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

Conditions

Planned to perform hip replacement surgery in the lateral position

Interventions

Group E:Using endotracheal tube to ventilation
Group L:Using adjustable visual laryngeal mask to ventilation

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. ASA grade: I-III; 3. Elective lateral lateral hip replacement surgery under general anesthesia; 4. Planned surgical time < 2h; 5. Planned to removed the endotracheal tube immediately after surgery; 6. The patient have signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1. Mallampati classification > II; 2. BMI > 30kg/m^2; 3. Patients with the possibility of reflux aspiration; 4. Cardiac insufficiency or combined with cardiopulmonary diseases; 5. Have a history of respiratory infection within one month before the operation and have not quit smoking; 6. Patients with anticipated and unanticipated difficult airway(Mouth opening degree < 2 transverse fingers, limited neck movement, and previous history of radiotherapy for the pharyngeal and cervical regions); 7. Have a history of head and neck surgery;

Design outcomes

Primary

MeasureTime frame
Effective ventilation rate;

Secondary

MeasureTime frame
Complications associated with artificial airway insertion;The lowest SpO2 during inserting a visual laryngeal mask/tracheal tube;The number of adjust artificial airways during the operation;complication (Hoarseness and sore throat);The number of artificial airway insertions;The rate of laryngeal mask displacement;Hemodynamic parameters;The time of artificial airway established;The time of artificial airway removed;Ventilator parameters (parameters related to respiratory mechanics);

Countries

China

Contacts

Public ContactHai Yu

West China Hospital of Sichuan University

yuhai@scu.edu.cn+86 18980601548

Outcome results

None listed

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