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The Effects of Different Airway Devices on Middle Ear Pressure in Pediatric Patients

A

Adiyaman University Research Hospital

Status

Unknown

Conditions

Simple Ear
Local Pressure Effects

Treatments

Device: Supreme laryngeal mask application
Device: Cobra laryngeal mask application
Device: I-gel laryngeal mask application
Device: Laryngeal mask classical application
Device: Proseal laryngeal mask application

Study type

Interventional

Funder types

Other

Identifiers

NCT02334072
Adiyaman/LMA-MEP

Details and patient eligibility

About

Even though the effects of anesthetic agents both inhalation and intravenous have been well described, the effect of laryngeal mask airways haven't. The purpose of the study is to determine the effects of different types of laryngeal mask airways on middle ear pressure.

Full description

All the patients in each group of laryngeal mask airway will contain 20 patients. In all groups middle ear pressures will be measured, in both right and left ear, preoperatively, after induction of anesthesia, insertion of laryngeal mask and in 1st., 5th., 10th. minutes and every 5 minutes perioperatively and recorded. Also the heart rates,arterial oxygen saturation (SaO2), airway pressures and end-tidal carbon dioxide values will be recorded before and following induction of anesthesia and in 1st., 5th., 10th. minutes and every five minutes perioperatively. Patients will be followed during the hospital stay for any complications.In all groups premedication will be done with midazolam. Anesthesia will be inducted with propofol and fentanyl; and maintained with sevoflurane-air combination.

Enrollment

100 estimated patients

Sex

All

Ages

1 day to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective patients undergoing subumbilical surgery under general anesthesia

Exclusion criteria

  • Emergency conditions
  • Rejection of patient approval
  • Tympanic membrane perforation history
  • Anticipated difficult airway
  • Contraindications for LMA application

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

100 participants in 5 patient groups

Classical
Experimental group
Description:
Laryngeal mask airway (LMA) is manufactured from medical grade silicone rubber and is reusable. It consists of 3 main components: An airway tube, inflatable mask and mask inflation line. The airway tube is slightly curved to match the oropharyngeal anatomy, semirigid to facilitate atraumatic insertion and semitransparent, so that condensation and regurgitated material is visible. The distal aperture of the airway tube opens into the lumen of an inflatable mask and is protected by two flexible vertical rubber bars, called mask aperture bars, to prevent the epiglottis from entering and obstructing the airway. The laryngeal mask classical application will be done following anesthesia induction.
Treatment:
Device: Laryngeal mask classical application
I-Gel
Experimental group
Description:
I-Gel LMA is anatomically designed mask made of a gel-like thermoplastic elastomer. It has a drain tube for gastric aspiration. I-gel laryngeal mask application will be done following anesthesia induction.
Treatment:
Device: I-gel laryngeal mask application
Cobra
Experimental group
Description:
Cobra LMA consists of a translucent silicone airway tube with an inflatable cuff sited approximately two-thirds of the way to the tip, a 15-mm standard adapter and an expanded distal end with a smooth posterior surface. The cuff forms a seal in the upper pharynx and the distal end sits in the laryngopharynx. The distal grill is designed to sit over the laryngeal inlet.Cobra laryngeal mask application will be done following induction of anesthesia
Treatment:
Device: Cobra laryngeal mask application
Supreme
Experimental group
Description:
The Supreme LMA is a single-use polyvinyl chloride supraglottic device. High oropharyngeal leak pressures are important as they indicate airway protection, feasibility of positive pressure ventilation and likelihood of successful LMA placement.Supreme laryngeal mask application will be done following induction of anesthesia and anesthesia.
Treatment:
Device: Supreme laryngeal mask application
Proseal
Experimental group
Description:
The ProSeal LMA is the most complex of the specialized laryngeal mask devices.The primary design goal was to construct a laryngeal mask with improved ventilatory characteristics that also offered protection against regurgitation and gastric insufflation. The principal new features are a modified cuff and a drain tube.Proseal laryngeal mask application will be done following induction of anesthesia and anesthesia.
Treatment:
Device: Proseal laryngeal mask application

Trial contacts and locations

1

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Central trial contact

Ülkü Sabuncu; Ruslan Abdullayev

Data sourced from clinicaltrials.gov

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