Dexmedetomidine vs Propofol-lidocaine Mixture in Preventing the Post Operative Emergence Agitation Following Sevoflurane Anasthesia

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age2-8
SponsorSohag University

About this trial

Primary we will Compare the Efficacy between Dexmedetomidine and "Propofol-lidocaine" mixture in preventing the post operative emergence agitation following sevoflurane anasthesia in pediatric ophthalmic surgeries Secondary we will evaluate time of extubation, time of orientation, Hemodynamic variables, Visual analog scale ( VAS), facial expressions scale , Adverse events

Eligibility criteria

Qualifiers

patients aged 2-8 years .

ASA physical status I-II.

Scheduled for elective surgeries under general anesthesia with sevoflurane

Disqualifiers

History of psychiatric illness or cognitive impairment.

Known allergy to study drugs.

Severe cardiovascular, hepatic, or renal disease.

Chronic use of sedatives or opioids.

Trial design

Treatments tested in this trial

  • Dexmedetomidine
  • Propofol
  • Placebo

Treatment groups

200 Participants
are divided into 3 treatment groups

Locations

This trial has no locations

Sponsors and collaborators