Clinical study of SACOVLMTM and Supreme in laparoscopic abdominal surgery
Conditions
Interventions
Supreme group (S?):Insertion of Supreme after induction of general anesthesia
SACOVLM group (M group):Insertion of SACOVLM after induction of general anesthesia
Sponsors
The First Affiliated Hospital of Shandong First Medical University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Those who are older than 18 years old; 2. American Society of anesthesiologists (ASA) grade I ~ III; 3. Patients scheduled for laparoscopic abdominal surgery under general anesthesia; 4. The patients and their families agree and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients allergic to any narcotic drugs; 2. Patients with severe respiratory diseases; 3. Patients with full stomach or clear risk of reflux aspiration, pregnancy or head and neck tumor; 4. Oropharyngeal deformity and laryngopharyngitis in patients with abnormal head and neck activity; 5. Predicted difficult airway (such as Mallampati grade 3-4, distance between nail and chin = 35kg / m2), severe obstructive sleep apnea syndrome, etc.); 6. Patients with severe systemic diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| oropharyngeal leak pressure;Peak airway pressure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of tracheal intubation;endoscopic view grading system of laryngoscopic view;Whether the implantation of gastric tube was successful or not;Time for removal of laryngeal mask;Vital signs;Laryngeal mask related complications; | — |
Countries
China
Contacts
Public ContactSun Yongtao
The First Affiliated Hospital of Shandong First Medical University
Outcome results
None listed