Anesthesiology and Reanimation Dept. Ordu University Training and Research Hospital
Altinordu, Ordu, 52100, Turkey (Türkiye)
NCT Number: NCT02186990
The purpose of this study is to evaluate the effect of propofol, etomidate and propofol-etomidate combination on hemodynamic responses during laryngoscopy and tracheal intubation and assess the adverse effect related to this drugs.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 4
Altinordu, Ordu, 52100, Turkey (Türkiye)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
2,5 mg/kg
0,3 mg/kg
0,15 mg/kg etomidate + 1,25 mg/kg propofol
Time frame: in ten minutes after intubation
e.g., heart rate, blood pressure (mean arterial pressure)
Time frame: within in 30 minutes drug administration
e.g. myoclonus, injection pain, allergy, skin rash
Ordu University
Other
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