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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05523752
Other study ID # 2022/03-13
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date August 15, 2022

Study information

Verified date August 2022
Source Zonguldak Bulent Ecevit University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date August 15, 2022
Est. primary completion date July 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Proseal Laryngeal Mask
insertion of Proseal Laryngeal Mask
Classic Laryngeal Mask
insertion of Classic Laryngeal Mask
I-gel
insertion of I-gel
Suprema Laryngeal Mask
insertion of Suprema Laryngeal Mask

Locations

Country Name City State
Turkey Zonguldak Bülent Ecevit University Zonguldak Kozlu

Sponsors (1)

Lead Sponsor Collaborator
Zonguldak Bulent Ecevit University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary difficulty of attempts pointing the difficulty of insertion from 0 to 100 during insertion procedure
Secondary Time of attempts time from insertion to ventilation during insertion procedure
Secondary number of attempts number of attempts for successfull placement during insertion procedure
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