Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | Dexmedetomidine | sedative and might be analgesic drug |
| DRUG | Nalbuphine | agonist antagonist narcotic |
| DEVICE | infusion pump | infusion 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.