Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07450495

Effect of Different Concentrations of Sevoflurane for Anesthesia Induction in Pediatric Ophthalmic Surgery

Effectiveness and Safety of 6% Versus 8% Sevoflurane for Anesthesia Induction in Pediatric Ophthalmic Minor Surgery: A Randomized Controlled Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Joint Shantou International Eye Center of Shantou University and the Chinese University of Hong Kong · Academic / Other
Sex
All
Age
1 Year – 6 Years
Healthy volunteers
Not accepted

Summary

This randomized controlled trial aims to compare the effectiveness and safety of 6% versus 8% sevoflurane inhalation induction in pediatric patients undergoing minor ophthalmic surgery. The primary outcome is emergence agitation assessed using the Pediatric Anesthesia Emergence Delirium (PAED) scale. Secondary outcomes include hemodynamic parameters, induction time, recovery time, and adverse events.

Conditions

Interventions

TypeNameDescription
DRUGSevofluraneSevoflurane inhalation anesthesia was used for induction and maintenance of general anesthesia in pediatric patients undergoing minor ophthalmic surgery.

Timeline

Start date
2025-02-25
Primary completion
2026-02-25
Completion
2026-04-01
First posted
2026-03-04
Last updated
2026-03-04

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07450495. Inclusion in this directory is not an endorsement.