Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Analgesia
Type
Interventional
Phase
Phase 1Phase 2
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Outcomes Assessor)Primary Purpose: Treatment

Participation Requirements

Age
Between 6 years and 18 years
Gender
Both males and females

Description

Site of study: This study will be carried out in neurosurgical operating rooms of Zagazig University Hospitals. b. Sample size: The sample size was calculated using OPEN EPI program assuming that the mean postoperative opioid intake among dexmedetomidine group was 0.3±0.2 mg/kg and among lidocaine g...

Site of study: This study will be carried out in neurosurgical operating rooms of Zagazig University Hospitals. b. Sample size: The sample size was calculated using OPEN EPI program assuming that the mean postoperative opioid intake among dexmedetomidine group was 0.3±0.2 mg/kg and among lidocaine group was 0.58± 0.4 so at power of study 80% confidence interval 95%, the sample size was calculated to be 42 cases (21in each group ).

Tracking Information

NCT #
NCT04535089
Collaborators
Not Provided
Investigators
Principal Investigator: Alshaimaa Kamel, M.D Zagazig University