Comparison of I-Gel Laryngeal Mask Airway Placement Methods in Elective Surgery
- Conditions
- Effective I -Gel Mask Airway Placement Technique
- Interventions
- Other: i-gel placement maneuvers
- Registration Number
- NCT03542032
- Lead Sponsor
- Ankara Diskapi Training and Research Hospital
- Brief Summary
To compare the jaw thrust maneuver with the conventional technical methods to place the I-Gel laryngeal mask
- Detailed Description
Patients who underwent elective surgery under general anesthesia and who were between the ages of 18 and 75 and who had ASA score I-II-III would be included in the study. Patients' mallampati scores, thyromental distances, mouth openings will be recorded.
Patients will be divided into two groups according to supraglottic airway insertion method.
Both groups will record the insertion time of i-gel, number of trials, operative time, placement complications.
Recorded complications (blood, laryngospasm, etc.) during insertion and removal of supraglottic airway devices will be assessed.
Patients' postoperative sore throat will be questioned and recorded.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 98
- Patients between the ages of 18 and 75 years
- American Society of Anesthesiologists I, II or III
- Those with anatomical disorders related to the upper airway
- lung disease
- gastric regurgitation
- Those who have had lung infection in the last 3 weeks
- Supraglottic airway vehicle not settled
- Those who are hired for any reason
- EtCO2> 45
American Society of Anesthesiologists 4 or 5
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description jaw-thrust i-gel placement maneuvers the i-gel was inserted with triple airway maneuver (mouth opening, head extension and jaw thrust) This groups will record the insertion time of i-gel, number of trials, operative time, placement complications. Recorded complications (blood, laryngospasm, etc.) during insertion and removal of supraglottic airway devices will be assessed. Patients' postoperative sore throat will be questioned and recorded.
- Primary Outcome Measures
Name Time Method successful insertion number 2 minutes successful insertion number
insertion time 2 minutes Time for successful i-gel insertion
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Diskapi Yildirim Beyazit Training Research Hospital
🇹🇷Ankara, Turkey