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Clinical Trial Summary

The objective of this study is to compare the physiologic resolution of dental infections between immediate tooth extraction (control group) and administration of systemic antibiotics and delayed extraction (study groups 1 and 2). A secondary objective is two compare two different antibiotic regimens in the delayed extraction groups (study group 1 and 2).


Clinical Trial Description

This is a prospective partially randomized clinical trial. Patients 2-11 years old who have a vestibular swelling associated with an odontogenic infection are being studied. Subjects will self-select into the control or study group. All subjects will be offered to have the tooth extracted on the day of diagnosis, and if this treatment is chosen they will join the control group (group 1). Subjects who defer treatment will be placed on amoxicillin and will be placed into the study group. The study group will be randomized into two parallel study groups that either have average dose antibiotics for 10 days (group 2), or maximum dose antibiotics for 5 days (group 3). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04057014
Study type Interventional
Source Boston Children's Hospital
Contact
Status Withdrawn
Phase Phase 4
Start date October 2020
Completion date October 2, 2020

See also
  Status Clinical Trial Phase
Completed NCT02141217 - AUGMENTIN™ in Dental Infections Phase 4