About this trial
This study is designed to evaluate the effectiveness of ultrasound-guided greater auricular nerve block (GAN) on the reduction of emergence agitation (EA) occurrence and EA severity in children who are receiving general anesthesia for a microscopic middle ear operation.
Eligibility criteria
Qualifiers
Age between 5 and 14 years (preschool to early school age group at highest risk for EA).
ASA physical status I or II.
Scheduled for elective microscopic middle ear surgery under general anesthesia (e.g., tympanoplasty, myringoplasty).
Ability to comply with FLACC and PAED scoring during postoperative period.
Disqualifiers
Known neurological, developmental, or psychiatric disorders (e.g., autism, ADHD, seizure disorder).
Known hypersensitivity to amide local anesthetics (e.g., lidocaine, bupivacaine).
Skin infection, hematoma, or trauma at or near the proposed block site.
Non-elective (emergency) or combined surgeries.
Trial design
Treatments tested in this trial
- ultrasound-guided greater auricular nerve block (GANB)