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Clinical Trial Summary

59 medically healthy patients, who are scheduled for third molar extraction surgery and give informed consent for the trial, are operated using a split-mouth technique. One group of patients will be assigned to the test group (Amoxilan) for the first surgery and to the control group (placebo) for the second surgery, and vice versa, according to randomisation. Patients receive 8 capsules Amoxilan or placebo (according to randomisation) perioperatively, and 6 capsules Amoxilan/placebo per day for 3 days postoperativeley.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05142449
Study type Interventional
Source Medical University of Graz
Contact
Status Completed
Phase Phase 4
Start date March 25, 2019
Completion date September 1, 2022