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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


Study Design

Related Conditions & MeSH terms

NCT number NCT05126459
Study type Interventional
Source Loma Linda University
Contact Jung-Wei Chen, DDS,MS,PhD
Phone (909) 558-4690
Email [email protected]
Status Not yet recruiting
Phase Phase 3
Start date November 2021
Completion date December 2023

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