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Clinical Trials/NCT05523752
NCT05523752CompletedNot Applicable

Placement of Four Different Supraglottic Airway Devices by Medicine Faculty Students: A Manikin Study

Zonguldak Bulent Ecevit University1 site in 1 country1 target enrollmentStarted: March 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
1
Locations
1
Primary Endpoint
difficulty of attempts

Study Overview

Brief Summary

When tracheal intubation and face mask ventilation fail, and the insertion of supraglottic airway devices (SHA) can provide ventilation, protecting the patient from hypoxemia. Supraglottic airway devices have become an important part of difficult airway algorithms. The European Resuscitation Council Guidelines recommend supraglottic airway devices for airway management by non-specialized healthcare providers. Education through simulators contributes to the development of students without direct contact with patients. In this study, it was aimed to compare the success of placement of four different supraglottic airway devices on the manikin of term 5 students who participate to the Anesthesiology and Reanimation internship.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Studying in medical school in term 5
  • •To have completed anesthesiology and reanimation internship

Exclusion Criteria

  • •who do not want to participate in the study
  • •Students with previous experience with four airway devices

Arms & Interventions

Proseal Laryngeal Mask

Other

Intervention: Proseal Laryngeal Mask (Device)

Classic Laryngeal Mask

Other

Intervention: Classic Laryngeal Mask (Device)

I-gel

Other

Intervention: I-gel (Device)

Suprema Laryngeal Mask

Other

Intervention: Suprema Laryngeal Mask (Device)

Outcomes

Primary Outcomes

difficulty of attempts

Time Frame: during insertion procedure

pointing the difficulty of insertion from 0 to 100

Secondary Outcomes

  • Time of attempts(during insertion procedure)
  • number of attempts(during insertion procedure)

Investigators

Sponsor
Zonguldak Bulent Ecevit University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Keziban Bollucuoglu

anesthesiologist

Zonguldak Bulent Ecevit University

Study Sites (1)

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