A Comparative Study on the Effects of Esmolol and Lidocaine about agitation After pediatric strabismus surgery: a double-blind, randomized clinical study

A Comparative Study on the Effects of Esmolol and Lidocaine about agitation After pediatric strabismus surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0008195

Enrollment

100

Registered

2023-02-16

Start date

2019-01-16

Completion date

Unknown

Last updated

2023-03-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : in Group EL, lidocaine 2 mg/kg was administered immediately after surgery and esmolol 0.5 mg/kg was administered when the patients voluntarily moved after turning the anesthetic gas off and the

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: pediatric patients aged 5–9 years who were scheduled to undergo strabismus surgery

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
Agitation	—

Secondary

Measure	Time frame
Blood pressure Heart rate	—

Countries

Korea, Republic of

Contacts

Public ContactJi Jae Young

Soon Chun Hyang University Hospital Cheonan

phmjjy01@hanmail.net+82-41-570-2114

Outcome results