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Clinical Trial Summary

The main objective of this study is to evaluate the effectivity of intranasal dexmedetomidine sedation during intra-articular injection therapy. Intranasal dexmedetomidine is compared with dinitrous oxide (N2O) which has already been proven safe and effective sedation method during painful procedures in pediatric patients. In earlier studies the median VAS during intra-articular corticosteroid injections with patients receiving nitrous oxide has been 3 (Uziel et al 2008). Study hypothesis is that with intranasal dexmedetomidine sedation the VAS pain levels will be 1 unit lower.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03069638
Study type Interventional
Source University of Oulu
Contact
Status Completed
Phase Phase 4
Start date February 1, 2017
Completion date December 18, 2023

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