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.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 2 Years to 12 Years |
| Sex | All |
| Enrollment | 114 (estimated) |
| Sponsor | Pakistan Institute of Medical Sciences Government |
| Locations | 1 site (Islamabad, Federal) |
| Status | Recruiting |
| Started | August 28, 2026 |
| Main results expected | November 28, 2026 |
| Study ends | November 28, 2026 |
| Registry record updated | September 2, 2026 |
| Trial ID | NCT07799311 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 \- 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
- Study coordinator: Muhammad Haroon Principal Investigator, MBBS, FCPS
- Email: haroonanwar22@gmail.com
- Phone: +92-333-5236956
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.