Clinical Trials Directory

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UnknownNCT04058899

Dexmedetomidine Versus Nalbuphine in Prevention of Emergence Agitation Following Adenotonsillectomy in Pediatrics

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
120 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
All
Age
2 Years – 5 Years
Healthy volunteers
Not accepted

Summary

The aim of the present study is to compare the effect of IV infusion 0.5 µg/kg dexmedetomidine and IV 0.1 mg/kg nalbuphine in preschool children for prevention of emergence agitation after adenotonsillectomy under sevoflurane anesthesia.

Detailed description

Consent will be obtained from legal guardian of children,patients will be randomized according to computer randomization to one of two groups, dexmedetomidine group (DEX)group who will receive 0.5 µg/kg dexmedetomidine diluted in 50 ml of normal saline 0.9% to be given by IV infusion over 10 minutes after induction of anesthesia then 5ml of 0.9% normal saline IV ,nalbuphine group (NAL)group will receive IV infusion of 50 ml of 0,9%normal saline by IV infusion over 10 minutes then 0.1mg/kg nalbuphine diluted in 5ml of 0.9%normal saline IV after induction of anesthesia.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidinesedative and might be analgesic drug
DRUGNalbuphineagonist antagonist narcotic
DEVICEinfusion pumpinfusion pump for titration of fluid containing drug infusion

Timeline

Start date
2019-03-05
Primary completion
2019-09-01
Completion
2019-09-01
First posted
2019-08-16
Last updated
2019-08-20

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04058899. Inclusion in this directory is not an endorsement.