Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 2 to 12

Propofol vs. Dexmedetomidine for Preventing Emergence Agitation in Children After Sevoflurane Anesthesia

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

Run by Pakistan Institute of Medical Sciences · NCT07799311 · Data updated 2026-11-12

This trial tests whether a single dose of propofol or a single dose of dexmedetomidine, given after surgery, better prevents emergence agitation in children recovering from sevoflurane anesthesia.

More Emergence Delirium trials

Quick facts

PhasePhase 4
Study typeInterventional
Ages2 Years to 12 Years
SexAll
Enrollment114 (estimated)
SponsorPakistan Institute of Medical Sciences
Government
Locations1 site (Islamabad, Federal)
StatusRecruiting
StartedAugust 28, 2026
Main results expectedNovember 28, 2026
Study endsNovember 28, 2026
Registry record updatedSeptember 2, 2026
Trial IDNCT07799311 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are children aged 2–12 years undergoing elective inguinal hernia repair with sevoflurane anesthesia.

Probably not a fit

Patients who do not experience emergence agitation or who have contraindications to either drug may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized, phase 4 trial compares propofol to dexmedetomidine administered at the end of surgery in children aged 2–12 undergoing elective inguinal hernia repair under general anesthesia. Emergence agitation is measured using the PEAD scale at 0, 5, 10, 15, and 30 minutes in recovery, with a score over 10 indicating agitation. The study aims to determine which drug more effectively reduces post-anesthesia behavioral disturbances.

Why it matters

Potential benefit: If successful, the approach could reduce postoperative agitation, improving safety and comfort for children and easing recovery for caregivers.

How similar studies have gone: Previous work has explored similar strategies for managing emergence phenomena, with varying results depending on patient population and anesthesia.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1- age 2-12 years 2-elective inguinal hernia repair under general anesthesia

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Exclusion Criteria:

1. congenital anomalies
2. allergic to study medications
3. chronic pain syndromes
4. malnourishment -

Where it's running

  • Pakistan Institute of Medical Sciences
    Islamabad, Federal, Pakistan
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.