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Trials / Completed

CompletedNCT03725930

Premedication by Clonidine Intranasal in Pediatric Surgery

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
90 (actual)
Sponsor
University Hospital, Lille · Academic / Other
Sex
All
Age
1 Year – 5 Years
Healthy volunteers
Accepted

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)

Conditions

Interventions

TypeNameDescription
DRUGClonidineclonidine intranasal premedication in preschool infants
OTHERPlaceboPlacebo intranasal premedication

Timeline

Start date
2019-03-26
Primary completion
2021-11-24
Completion
2023-11-24
First posted
2018-10-31
Last updated
2025-12-23

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03725930. Inclusion in this directory is not an endorsement.

Premedication by Clonidine Intranasal in Pediatric Surgery (NCT03725930) · Clinical Trials Directory