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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04509453
Other study ID # UNUD-CTR-FK270720-003
Secondary ID 1320/UN14.2.2.VI
Status Completed
Phase N/A
First received
Last updated
Start date August 30, 2020
Est. completion date November 1, 2020

Study information

Verified date December 2020
Source Udayana University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Various techniques have been developed to get a good LMA position, one of them is using a laryngoscope. The most popular laryngoscope used for LMA installation is the Macintosh type. Technological developments have brought laryngoscopes into the video era, one of which is McGRATH's laryngoscope, which from several studies about having an advantage in terms of the first attempt, time, complications, and hemodynamic stability of intubation. It needs to be proven through research on the comparison of clinical outcomes of LMA installation with McGrath laryngoscope and Macintosh laryngoscope.


Recruitment information / eligibility

Status Completed
Enrollment 102
Est. completion date November 1, 2020
Est. primary completion date October 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Patients underwent surgery with general anesthesia by LMA insertion in Sanglah General Hospital - Agreed to be included in the study by signing informed consent - American Society of Anesthesiologist physical status 1-2 Exclusion Criteria: - Patients unfit for LMA insertion - Patients with suspected airway management difficulty - Pregnancy - Morbid obese

Study Design


Related Conditions & MeSH terms


Intervention

Device:
McGRATH laryngoscopy
Patients who underwent general anesthesia with LMA insertion by using McGRATH video layngoscopy
Macintosh laryngoscopy
Patients who underwent general anesthesia with LMA insertion by using classic Macintosh video layngoscopy

Locations

Country Name City State
Indonesia Sanglah General Hospital Denpasar Bali

Sponsors (1)

Lead Sponsor Collaborator
Udayana University

Country where clinical trial is conducted

Indonesia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with first-attempt success Successful LMA insertion within first attempt immediately after LMA insertion
Primary Mean arterial pressure Mean arterial pressure measured by non-invasive blood pressure monitor immediately after LMA insertion
Primary Heart rate Heart rate measured by standard monitor immediately after LMA insertion
Secondary Time required Time required for LMA insertion using the respective method immediately after LMA insertion
Secondary Complications Incidence of hoarseness or throat pain due to LMA insertion An hour after the the end of surgery
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