A Comparative Study on the Effects of Esmolol and Lidocaine about agitation After pediatric strabismus surgery: a double-blind, randomized clinical study
Not Applicable
Completed
- Conditions
- Injury, poisoning and certain other consequences of external causes
- Registration Number
- KCT0008195
- Lead Sponsor
- Soon Chun Hyang University Hospital Cheonan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
pediatric patients aged 5–9 years who were scheduled to undergo strabismus surgery
Exclusion Criteria
presence of mental illness such as excessive anxiety or cardiac or respiratory disease; presence of adverse reactions to lidocaine or esmolol; or the patient’s or guardian’s refusal to participate in the study. Moreover, patients who were excessively unstable before surgery or had a low HR, fever or cough, or persistent tachycardia and had to receive perioperative esmolol continuously during surgery were excluded from the study even if they consented to participate, since these conditions could affect the results of the study.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Agitation
- Secondary Outcome Measures
Name Time Method Blood pressure Heart rate