drugset / Trial / NCT03647579

Dexmedetomidine Versus Midazolam Added to Ketamine in Pediatric Patients Undergoing Bone Marrow Aspiration and Biopsy

NCT03647579 ↗

Completed 100 enrolled Assiut University
RandomizedParallel-groupDouble-blindTreatment

Summary

Group I :The patients will receive midazolam intravenously (i.v.) in a dose of 0.05 mg/kg diluted by 50ml saline over 10 minutes using syringe pump plus 1 mg/kg ketamine (iv). Group II : The patients will receive Dexmedetomidine intravenously (i.v.) in a dose of 2mic/kg diluted by 50ml saline over 10 minutes using syringe pump plus 1 mg/kg ketamine (iv). The objective of this study to evaluate the clinical effects, adverse effects and recovery time of two different sedative agents (midazolam and Dexmedetomidine) combined with ketamine during conscious sedation for child patient with haematological cancer undergoing BMA \&biopsy.

Timeline

Start
2018-08-30
Primary completion
2018-12-15
Completion
2019-04-20

Drugs

EvaluationDrugModalityDoseRoute
Comparator Dexmedetomidine Other / unclassified 2 ug/kg Intravenous
Comparator Midazolam Small molecule 0.05 mg/kg Intravenous
Comparator Ketamine Small molecule 1 mg/kg Intravenous

Indications

No indication recorded.