Airway Management Clinical Trial
Official title:
Head Position for Laryngeal Mask Air Leak and Performance in Paediatric Patients (Neutral, Sniffing and Beyond Sniffing Position): Prospective Randomized Trial
The correct head position for airway management is considered as a mainstay of good clinical practice. The recommended head position for all patients is the horizontal position of the head with in tragus-to- sternal notch in line alignment. This could be achieved in infant (under two years) supporting the shoulder, neutral head positioning in children between 2-8 (12) years and with so called "sniffing position" (SP) in patients over 12 year by supporting the head (i.e. with pillow) to reach the proper alignment (tragus to sternal notch). Although, this could be considered as gold standard, there are currently insufficient high quality evidence-based data to confirm the association between the better laryngeal view during the direct laryngoscopy and tragus-to-sternal notch position. Recently, "beyond sniffing" position was described as further head elevation (compared to sniffing position) in adult patients. Beyond sniffing position was associated with superior laryngeal inlet visualization compared to standard sniffing position in common elective adult airway management (patients with suspected or confirmed difficult airway was excluded). The hypothesis of SNIFF LM trial is that the sniffing position or even beyond sniffing position could be associated with superior laryngeal mask performance (lower incidence of air leak, LM easier introduction) compared neutral position in paediatric patients undergoing elective paediatric anaesthesia
Paediatric patients (between 2-18 years) undergoing elective airway management without predicted/confirmed difficult airway will be eligible for inclusion. The patients will be screened for eligibility during the preanaesthesia visit in anaesthesiology examination room. After informed consent the patients will be randomized into 3 groups (according to the induction head position) - neutral head position (without head elevation, head supported with the hollow foam circle to prevent side head movement), sniffing position (head support with inflatable pillow the reach the horizontal in-line alignment of tragus-to-sternal notch line) and beyond sniffing position (further 25% increase of head support compared to sniffing position). The randomization will be performed by the Institute of Biostatistics and Analysis in form of sealed envelopes. The group allocation will be 1:1:1. After fulfilling the inclusion criteria and obtaining the informed consent the patient will be randomized into 3 groups. Before anaesthesia induction the head of the patient will be positioned into the predefined position according to the results of randomization. The anaesthesia induction could be performer either inhalation or intravenous route. After anaesthesia induction, the laryngeal mask will be inserted in the selected position. After laryngeal mask insertion, stabilisation of vital signs and of anaesthesia depth, the measurement will be intiated within 5 minutes. After one minute of ventilation 3 leak volumes (inspiration - expiration tidal volume) together with the peak airway pressure (3 measurements) will be recorded (the mean volume and mean pressure will be analyzed). Patient´s head will be repositioned into the 2nd position and after one minute of ventilation leak volume and airway pressure will be recorded as previously described, after measurement, the head position will be repositioned into the 3rd positon and the measurement will be repeated. The incidence of 1st insertion attempt failure rate, incidence of laryngeal mask failure rate, incidence of the need for reposition will be recorded together with the incidence of airway related complications. ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03908411 -
The Effect of Paratracheal Pressure on the Glottic View
|
N/A | |
Completed |
NCT04564105 -
Simulation Training and Teamwork Concerning Intubation on the Icu
|
N/A | |
Completed |
NCT02988336 -
TMHT - New Method of Difficult Intubation Prediction
|
N/A | |
Completed |
NCT03002857 -
Comparison of I-gel LMA, Classical LMA With a New Supraglottic Airway the Baska Mask® in Urological Surgery
|
N/A | |
Recruiting |
NCT06337006 -
Laryngeal Mask Airway Failure in Pediatric Patients
|
||
Completed |
NCT03443219 -
RCT- LMA Supremeā¢ Versus the Spritztube® Tracheal Cannula in Anesthetized Adult Patients
|
N/A | |
Completed |
NCT05044416 -
VieScope in Patients With an Expected Difficult Airway
|
N/A | |
Not yet recruiting |
NCT05534451 -
Comparison Among Three Different Video Scope Guided Nasotracheal Intubation.
|
N/A | |
Recruiting |
NCT06073977 -
Risk Factors for Pediatric Difficult Supraglottic Airway Placement and Ventilation
|
||
Not yet recruiting |
NCT03687385 -
The Effect of High-flow Nasal Oxygenation to the Saturation During Analgo-sedation in Different ASA Risk Class Patients
|
N/A | |
Not yet recruiting |
NCT03687424 -
Can High-flow Nasal Oxygenation Improve Oxygen Saturation During Analgo-sedation in Obese Adults?
|
N/A | |
Enrolling by invitation |
NCT05055401 -
Airway Management Skills Amongst Anesthesia Providers
|
||
Terminated |
NCT02644837 -
AuraGain and iGel Crossover Comparison
|
N/A | |
Not yet recruiting |
NCT02920879 -
Airway Effects of PEEP During Anesthesia Induction.
|
N/A | |
Completed |
NCT02263300 -
Spatial Orientation and Fiberoptic Intubation Skills in the Novice: A Randomized Controlled Trial
|
||
Completed |
NCT01718561 -
The Difficult Airway Management Trial: "The DIFFICAIR-Trial"
|
N/A | |
Completed |
NCT01635660 -
Out-of-Hospital Randomized Comparison of Video-assisted Endotracheal Intubation
|
N/A | |
Completed |
NCT00956592 -
Clinical Evaluation of the Storz CMAC Laryngoscope
|
N/A | |
Completed |
NCT00892671 -
Airway Management and Vascular Access Simulation
|
N/A | |
Completed |
NCT03848559 -
Airway Management With Simulated Microgravity Using a Submerged Model
|
N/A |