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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05121701
Other study ID # ERZURUMSEHIR1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 30, 2021
Est. completion date March 1, 2022

Study information

Verified date March 2022
Source Van Bölge Egitim ve Arastirma Hastanesi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes a highly contagious infection with the highest viral load in the upper respiratory secretions. Despite using personal protective equipment, SARS-CoV-2 contamination to the healthcare personnel is possible during the airway management of infected patients. Direct laryngoscopy remains as the most common method for endotracheal intubation. Our study aimed to compare the use of video laryngoscopy with direct laryngoscopy for tracheal intubation in adult patients receiving general anesthesia for elective surgery during the COVID-19 pandemic.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date March 1, 2022
Est. primary completion date February 15, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - ASA I-II - Elective surgery Exclusion Criteria: - Intraoral or neck surgery - gastroesophageal reflux - delayed gastric emptying - pregnancy - scoliosis

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Videolaryngoscope
C-MAC PM-Karl Storz
Macintosh Laryngoscope
Laryngoscope

Locations

Country Name City State
Turkey Erzurum City Hospital Erzurum

Sponsors (1)

Lead Sponsor Collaborator
Van Bölge Egitim ve Arastirma Hastanesi

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Piepho T, Fortmueller K, Heid FM, Schmidtmann I, Werner C, Noppens RR. Performance of the C-MAC video laryngoscope in patients after a limited glottic view using Macintosh laryngoscopy. Anaesthesia. 2011 Dec;66(12):1101-5. doi: 10.1111/j.1365-2044.2011.06872.x. Epub 2011 Aug 25. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Intubation time Time from Beginning of Intubation to Full Ventilation of the Lungs First 5 minutes of the operation
Secondary Intubation Comfort Scale(0=bad, 1=moderate, 2=good 3=very good) First 5 minutes of the operation
Secondary Cormack-Lehane Scoring Scale(1= Full view of glottis, 2=Partial view of glottis 3=Only epiglottis seen, none of glottis seen 4=Neither glottis nor epiglottis seen) First 5 minutes of the operation
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