RecruitingPhase 4NCT07799311

Comparing the Efficacy of Propofol and Dexmedetomidine in Prevention of Emergence Agitation After Sevoflurane Anesthesia in Children

Comparison of Propofol and Dexmedetomidine in Prevention of Emergence Agitation After Sevoflurane Anesthesia Following Inguinal Hernia Repair: A Randomized Control Trial


Sponsor

Pakistan Institute of Medical Sciences

Enrollment

114 participants

Start Date

Aug 28, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This is a clinical study for comparing the efficacy of two drugs i.e propofol and dexmedetomidine in prevention of a group of post operative abnormal behaviours that can occur after sevoflurane anesthesia in children and we will measure this by a special scale which is used to evaluate these behavioural changes.


Eligibility

Min Age: 2 YearsMax Age: 12 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Dexmedetomidine and a drug called propofol 1mg/kg for people with emergence delirium, anesthesia. The study is currently recruiting participants at 1 location. People eligible for this study include aged 2 Years to 12 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGpropofol 1mg/kg

1mg/kg propofol given 10 minutes before the end of surgery

DRUGDexmedetomidine

0.3mcg/kg of dexmedetomidine to group D patients will be given after dilution with 10ml of 0.9%saline over 1 min given 10 minutes before extubation


Locations(1)

Pakistan Institute of Medical Sciences

Islamabad, Federal, Pakistan

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NCT07799311


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