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GMA-Tulip Laryngeal Mask Airway versus LAM Supreme Laryngeal Mask Airway in Airway Management for Lateral Decubitus Position During Laparoscopic Nephrectomy: A Randomized Controlled Superiority Trial

Comparison of GMA-Tulip Laryngeal Mask Airway versus LAM Supreme Laryngeal Mask Airway in Airway Management for Lateral Decubitus Position During Laparoscopic Nephrectomy: A Randomized Controlled Superiority Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118461
Enrollment
Unknown
Registered
2026-02-05
Start date
2026-02-15
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Laparoscopic Nephrectomy

Interventions

GMA Group:GMA-Tulip Laryngeal Mask Airway
LAM Group:LAM Supreme Laryngeal Mask Airway

Sponsors

The Second Hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–75 years; 2. Scheduled to undergo elective laparoscopic nephrectomy under general anesthesia (anticipated operative duration: 30–240 minutes); 3. American Society of Anesthesiologists (ASA) Physical Status Classification I–III; 4. Body mass index (BMI) 18.5–30 kg/m²; 5. Patient has provided informed consent and signed a written consent form.

Exclusion criteria

Exclusion criteria: 1. Presence of predictors for difficult airway (Modified Mallampati classification III–IV, inter-incisor distance <2.5 cm, thyromental distance <6 cm, severe limitation in neck mobility). 2. History of oropharyngeal surgery or anatomical abnormalities. 3. Gastroesophageal reflux disease, high risk of aspiration, or patients requiring rapid sequence induction. 4. Pre-existing respiratory conditions such as respiratory tract infection, chronic cough or hoarseness, chronic bronchitis, or asthma. 5. Current participation in other clinical studies.

Design outcomes

Primary

MeasureTime frame
Oropharyngeal Leak Pressure (OPLP);

Secondary

MeasureTime frame
Number of laryngeal mask insertion attempts;total duration of the insertion procedure;operator's subjective assessment (Good, Fair, Poor);Whether air leakage occurs at an airway pressure of 20 cmH2O;Whether air leakage occurs at an airway pressure of 25 cm H2O;Ventilation Quality Score During Mechanical Ventilation;Peak Airway Pressure and Plateau Pressure;Anatomical Alignment Classification: Includes 4-category grading and GMA grading;Oropharyngeal Leak Pressure (OPLP) when the head is turned to one side at 30° and 45°;Whether air leakage occurs;whether abnormal elevation of airway pressure occurs;whether hypoxemia occurs;whether position adjustment is performed and the number of adjustments;whether conversion to endotracheal intubation is required;Whether normal ventilation can be achieved after resuming spontaneous breathing and suctioning;whether blood is present upon removal of the laryngeal mask;whether hoarseness occurs;whether sore throat occurs;whether gastric fluid is present in the oropharynx;Whether hoarseness occurs within 24 hours postoperatively;whether reflux aspiration occurs within 24 hours postoperatively;whether pneumonia develops within 24 hours postoperatively;whether hypoxemia or atelectasis occurs within 24 hours postoperatively;

Countries

China

Contacts

Public ContactYingbin Wang

The Second Hospital of Lanzhou University

Wangyingbin6@163.com+86 139 9313 3264

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026