U.S., Oct. 27 -- ClinicalTrials.gov registry received information related to the study (NCT07894484) titled 'Lactium Premedication to Prevent Emergence Agitation' on Oct. 19.
Brief Summary: This biased coin sequential allocation, dose finding study will be conducted to determine the effective dose of oral lactium in 90% of children (ED90) for prevention of emergence agitation during recovery from adenotonsillectomy.
Study Start Date: Nov. 10
Study Type: INTERVENTIONAL
Condition:
Lactium
Premedication
Emergence Agitation
Adenotonsillectomy
Dose Finding Study
Intervention:
DRUG: Lactium
Lactium solution will be prepared by dissolving each one lentra sachet (150 mg lactium per sachet) in 50 ml of water so that each ml will contain 3 mg...