Clinical Trials Directory

Trials / Completed

CompletedNCT03174678

Dexmedetomidine Premedication in Children

The Effect of Oral Dexmedetomidine Premedication On Preoperative Cooperation and Emergence Delirium In Children Undergoing Dental Treatment

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Aydin Adnan Menderes University · Academic / Other
Sex
Age
2 Years – 6 Years
Healthy volunteers
Accepted

Summary

The aim of this retrospective study was to detect the effectiveness of 1µg/kg oral dexmedetomidine premedication on preoperative cooperation and emergence delirium of the the young children underwent complete dental treatment.

Detailed description

One Hundred children between the ages 2-6 years of ASA I status underwent full mouth dental rehabilitation were enrolled in the study. Group Dex (n=50) received 1µg/kg dexmedetomidine in apple juice and Group control (n=50) received apple juice only. Patients' Ramsey Sedation Scale (RSS), The Parental Seperation Anxiety Scale (PSAS), Mask Acceptance Scale (MAS) and Post anesthesia emergence delirium scale (PAEDS) and hemodynamic parameters were noted from their patient file. Premedication period was 45 minutes and measurements of RSS and hemodynamic parameters were recorded in baseline and every 15 minutes until the patients were transferred to the operating room. The data were analysed using the Kruskal-Wallis test, two sample t- tests, chi-square tests and ANOVA.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidine1µg/kg dexmedetomidine oral
OTHERapple juiceapple juice

Timeline

Start date
2017-03-01
Primary completion
2017-05-01
Completion
2017-05-25
First posted
2017-06-02
Last updated
2017-06-02

Locations

1 site across 1 country: Turkey (Türkiye)

Regulatory

Source: ClinicalTrials.gov record NCT03174678. Inclusion in this directory is not an endorsement.