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Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Procedural Sedation and Analgesia During Bone Marrow Aspiration and Biopsy

NCT number NCT03647579
Study type Interventional
Source Assiut University
Contact
Status Completed
Phase N/A
Start date August 30, 2018
Completion date April 20, 2019