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Clinical Trial Summary

This study will compare the post sedation events from three different multi-drug oral sedation regimens in order to help pediatric dentists determine the best course of action for their patients and prepare parents appropriately and caution them about the expected effects. Patients will be evaluated for adverse effects within two time periods at 8 and 24 hours post oral sedation procedure using surveys.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05126459
Study type Interventional
Source Loma Linda University
Contact
Status Completed
Phase Phase 3
Start date February 14, 2022
Completion date April 12, 2023

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