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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03279172
Other study ID # 22051012
Secondary ID
Status Completed
Phase N/A
First received August 7, 2017
Last updated September 11, 2017
Start date January 1, 2017
Est. completion date August 4, 2017

Study information

Verified date September 2017
Source Diskapi Teaching and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study was to compare intraocular pressure, intubation time, throat pain and hemodynamic variables using direct or videolaryngoscopy under general anesthesia requiring endotracheal intubation


Description:

INTRODUCTION Videolaryngoscopes are the new generation devices which were introduced into the difficult intubation algorithm by the American Society of Anaesthesiologists (ASA) in 2013 (1). Videolaryngoscopes are known to be superior to traditional direct laryngoscopy in cases of difficult airway, glottic visualisation is obtained more easily and less airway trauma is seen (2). Portable videolaryngoscope which is used in difficult airways (3). There are 2, 3, and 4 numbered blades. In the light source of the blade of the videolaryngoscope, there is a camera which is connected to a video screen monitor. In addition to passing soft tissues by visualisation, the camera is helpful in defining the glottic appearance (1).

There are studies which have compared the hemodynamic response and increase in IOP in intubation using direct laryngoscope and various videolaryngoscopes and airway devices . However, to the best of our knowledge there is no study comparing the effect on the increase in IOP of videolaryngoscope and direct laryngoscope. The aim of the current study was to compare IOP, hemodynamic parameters and throat pain in the use of videolaryngoscope and the direct laryngoscope.


Recruitment information / eligibility

Status Completed
Enrollment 78
Est. completion date August 4, 2017
Est. primary completion date August 3, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Elective Surgery under general anaesthesia

Exclusion Criteria:

- History of Glaucoma

- History of hearth disease

- History of Alzheimer

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
direct laryngoscope
procedure entubation
videolaryngoscope


Locations

Country Name City State
Turkey University of Health Diskapi Yildirim Beyazit Training and Hospital Ankara Altindag

Sponsors (1)

Lead Sponsor Collaborator
Diskapi Teaching and Research Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Griesdale DE, Liu D, McKinney J, Choi PT. Glidescope® video-laryngoscopy versus direct laryngoscopy for endotracheal intubation: a systematic review and meta-analysis. Can J Anaesth. 2012 Jan;59(1):41-52. doi: 10.1007/s12630-011-9620-5. Epub 2011 Nov 1. Review. — View Citation

Vinayagam S, Dhanger S, Tilak P, Gnanasekar R. C-MAC(®) video laryngoscope with D-BLADEā„¢ and Frova introducer for awake intubation in a patient with parapharyngeal mass. Saudi J Anaesth. 2016 Oct-Dec;10(4):471-473. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary High intraorbital pressure IOP 18-22 mmHg 1 minute
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