Clinical Trials Directory

Trials / Unknown

UnknownNCT04090944

Comparison Between Blind And Ultrasound Guided Laryngeal Mask Airway Insertion

Comparison Between Blind And Ultrasound Guided Laryngeal Mask Airway Insertion In Adult Patients Undergoing Elective Surgery: A Randomized Control Study

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
102 (estimated)
Sponsor
Beni-Suef University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The Proper position of a laryngeal mask airway (LMA) requires confirmation to ensure the adequacy of laryngeal seal and pulmonary ventilation. This confirmation may help in prevention of the peri-operative airway complication and ventilation events associated with LMA placement

Detailed description

It is common practice to inflate the cuff of LMA with the maximum recommended volume (size 3, 20 ml; size 4, 30 ml; size 5, 40 ml), as illustrated in several studies , but it may become more rigid which may cause displacement of the LMA and decreases the airway sealing of LMA, more pressure on pharyngeal mucosa which might cause severe mucosal ischemia leading to post- operative sore throat, dysphagia or hoarseness. Ultrasonography can reliably confirm correct placement of supraglottic devices like laryngeal mask airway (LMA) and rules out causes of inadequate ventilation , also it was found to be a sensitive in detecting rotational malposition of LMA in children. the replacement of air with saline in LMA cuffs enable detection of cuffs in the airway allowing visualization of the surrounding structures and tissues as the ultrasound beam can be transmitted through the fluid-filled cuffs without being reflected from air mucosal interface. the adequacy of LMA position will be confirmed by a fiberoptic laryngoscope (FOL)

Conditions

Interventions

TypeNameDescription
PROCEDUREthe fiberoptic laryngoscope (KARL STORZ 11301BN1, Germany) for confirmation of LMA position-The position of LMA will be assessed by another anesthetist (blinded assessor) using the fiberoptic laryngoscope (KARL STORZ 11301BN1, Germany) per the grading licensed by Aoyama et al.

Timeline

Start date
2019-10-01
Primary completion
2020-03-01
Completion
2020-03-01
First posted
2019-09-16
Last updated
2019-09-16

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04090944. Inclusion in this directory is not an endorsement.