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NCT04062747

The Effect Of I-Gel And Ambu Aura-I Use On Laryngofaryngeal Mucosa

Status unknown NA Last updated 20 August 2019
What this trial tests

NA trial testing I-gel in Mucosal Damage in 40 participants. Status unknown.

Timeline
18 May 2019
Primary endpoint
15 September 2019
20 September 2019

Quick facts

Lead sponsorBezmialem Vakif University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposescreening
Enrollment40
Start date18 May 2019
Primary completion15 September 2019
Estimated completion20 September 2019
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Bezmialem Vakif University

Who can join

Under 2, any sex, with Mucosal Damage. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Supraglottic airway devices (SGADs) are frequently preferred in surgical surgery for pediatric patients. i-gel LMA (laryngeal mask airway) and Ambu Aura-i LMA are the new generation supraglottic airway devices. The aim of this study was to compare airway trauma and postoperative complications due to i-gel and Ambu Aura in infants. In the study patients were divided into two groups performed on minor surgery ASA I (American Society of Anesthesiologists score) and 40 infants. After standard anesthesia i-Gel was placed into a group and Ambu Aura-i was placed to the other. Flexible bronchoscopy was performed at the end of surgery. Mucosal damage and postoperative complications in laryngopharyngeal structures were compared.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of I-gel

Trials testing the same drug.

Other Bezmialem Vakif University trials

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04062747.

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