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Clinical Trial Summary

There are few studies using intra nasal way to dispense premedication in pediatrics. This study will evaluate anxiolysis effect of Intranasal premedication with Clonidine vs Placebo. Two groups, randomized, Total of 150 patients (75 in each group) : Involvement in study for one patient : 7 days Duration of study including inclusion and data analysis : 18 months (inclusion 12 months; data analysis 6 months)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03725930
Study type Interventional
Source University Hospital, Lille
Contact Dina BERT, MD
Phone 3 20 44 60 69
Email dina.bert@chru-lille.fr
Status Recruiting
Phase Phase 3
Start date March 26, 2019
Completion date December 2023