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Clinical Trials/NCT03003598
NCT03003598
Completed
Not Applicable

The Effects of Endotracheal Intubation Via McGrath Videolaryngoscope on Intraocular Pressure

Inonu University0 sites50 target enrollmentDecember 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intraocular Pressure
Sponsor
Inonu University
Enrollment
50
Primary Endpoint
Systolic blood pressure
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

In this study, the investigators aimed to compare the effects of endotracheal intubation via direct laryngoscope (DLS) and McGrath Videolaryngoscope (VL) on intraocular pressure.

Detailed Description

Total of 50 American Society of Anesthesiologist Grade 1-2, Mallampati score 1 or 2, age between 18 to 65 patient planned to undergo nonopthalmic surgery will be included to study. Patients with glaucoma, diabetes mellitus, cardiovascular and pulmonary diseases, American Society of Anesthesiologist Grade III and IV, Body mass index more than 35, difficult intubation, undergo obstetrical surgery and propofol, fentanyl, rocuronium contraindicated will be excluded from the study. Patients will be divided randomly into 2 groups as direct laryngoscopic and videolaryngoscopic intubation group. Patients will be preoxygenated with %100 O2 for 3 minutes then anesthesia will be induced using propofol 2 mg / kg, fentanyl 1 mcg/kg, and rocuronium 0,5 mg / kg in both groups. After 3 minutes mask ventilation, patients will be intubated (women with No:7-7,5, men with No:8-8,5 intubation tube) by oral route. systolic blood pressure, diastolic blood pressure, mean arterial pressure, peripheral oxygen saturation, perfusion indexwill be recorded and intraocular pressure measured by ophthalmologist by tonopen device will be recorded pre-induction (basal), after induction, 1,2,3,5 minutes after intubation, respectively. Period between handling of laryngoscope or videolaryngoscope after termination of mask ventilation and obtain end tidal carbon dioxide will be accepted as application time and recorded. Study will be terminated after 5th minute values taken.

Registry
clinicaltrials.gov
Start Date
December 2016
End Date
April 4, 2017
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmet Selim Ozkan

M.D.

Inonu University

Eligibility Criteria

Inclusion Criteria

  • ASA (American Society of Anesthesiologist) Grade 1-2,
  • Mallampati score 1 or 2,
  • Age between 18 to 65,
  • Patient planned to undergo nonopthalmic surgery

Exclusion Criteria

  • Patients with glaucoma, diabetes mellitus, cardiovascular and pulmonary diseases, ASA Grade III and IV, BMI more than 35,
  • Patients with difficult intubation,
  • Patients undergoing obstetrical surgery and propofol, fentanyl, rocuronium contraindicated

Outcomes

Primary Outcomes

Systolic blood pressure

Time Frame: From Beginning of Anesthesia induction to 5th minutes of intubation

Heart rate

Time Frame: From Beginning of Anesthesia induction to 5th minutes of intubation

Intraocular pressure

Time Frame: From Beginning of Anesthesia induction to 5th minutes of intubation

Adverse events

Time Frame: within the first 24 hour after surgery

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