In this interventional double-blind randomized controlled trial (RCT), written informed consent was obtained from the infants' parents or guardians. The face mask was connected to a circle breathing system (Altech
® pediatric breathing circuit corrugated with water trap reference No. Al-1411.v002, Izmir, Turkey). After connecting the standard monitoring devices, general anesthesia was induced with 8% sevoflurane and 100% oxygen (flow = 2 - 3 lit/min) by the Dräger Fabius
® Plus anesthesia machine (Drägerwerk AG & Co. KGaA, Lübeck, Germany) using one of the mask-holding techniques (three-finger grip technique or three-finger grip plus submental maneuver) in the neutral position. After the patient was anesthetized and fell asleep within the first few seconds to one minute, the concentration of sevoflurane was reduced from 8% to 3.5% and maintained at this level. When the appropriate depth of anesthesia was reached, the anesthetist inserted an intravenous line, and the patient was intubated following administration of intravenous anesthetic drugs (sodium thiopental 5 mg/kg and fentanyl 1 mcg/kg). Spontaneous breathing was maintained for patients during the induction phase, and assisted ventilation was not performed. The duration of this process differed for each patient but fell in the range of 6 to 8 minutes. Demographic data (age, sex, weight, and height) for each patient was collected from their medical records. Quantitative hemodynamic parameters [systolic blood pressure (SBP), diastolic blood pressure (DBP), pulse rate (PR), O
2 saturation (SpO
2), and end-tidal CO
2 pressure (Et CO
2)] were measured. Also, VT
E was assessed quantitatively by the Drager machine and then classified into three groups of patient's quality of breath flow as either good, fair, or bad for VT
E in the range of 5 - 7 mL/kg, 3 - 5 mL/kg, and < 3 mL/kg, respectively (
10). Abnormal respiratory sounds and respiratory distress were evaluated by a single experienced anesthesiologist during mask ventilation. If any of the following situations occurred for a patient, the study was terminated, and necessary measures were taken: O
2 saturation drop below 95%, failure to manage the patient's airway, and the need to intubate the patient immediately.