Preemptive Oral Lactium Supplement to Prevent Emergence Agitation in Children Undergoing Adenotonsillectomy: A Randomized Placebo Controlled Study

Status: Recruiting
Location: See location...
Intervention Type: Other, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This prospective randomized controlled study will be conducted to evaluate the effects of preoperative lactium on the incidence and severity of emergence agitation in children undergoing adenotonsillectomy using sevoflurane anesthesia.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 7
Healthy Volunteers: f
View:

• Both gender

• 4 to 7 years age

• American Society of Anesthesiologists (ASA) Physical Status I or II

• Scheduled for adenotonsillectomy surgery under sevoflurane anesthesia

Locations
Other Locations
Egypt
Tanta University
RECRUITING
Tanta
Contact Information
Primary
Radwa E Eissa, MD
radwa.emad@med.tanta.edu.eg
01007473944
Time Frame
Start Date: 2025-09-22
Estimated Completion Date: 2026-02-25
Participants
Target number of participants: 130
Treatments
Experimental: Lactium group
cases will receive preoperative lactium, Lentra sachet (containing 150 mg Lactium) will be totally dissolved in 100 ml water and 50 ml will be given to cases, 2 hours before surgery.
Placebo_comparator: Control group
cases will receive 50 ml water added to it powdered vanilla flavor, 2 hours before surgery.
Related Therapeutic Areas
Sponsors
Leads: Tanta University

This content was sourced from clinicaltrials.gov