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Different Oral Doses of Clindamycin in Preventing Post-operative Sequelae of Lower Third Molar Surgery

Impacted Third Molar Tooth Clinical Trial

Official title:
Comparative Efficacy of Different Oral Doses of Clindamycin in Preventing Post-operative Sequelae of Lower Third Molar Surgery - a Randomized, Triple-blind Study

Clinical Trial Summary

The objective of the study is to determine the effect of antibiotic prophylaxis with three different doses of clindamycin on preventing infection and other complications after surgical extraction of impacted mandibular third molars.

Clinical Trial Description

The objective of the study is to determine the effect of antibiotic prophylaxis with three different doses of clindamycin on preventing infection and other complications after surgical extraction of impacted mandibular third molars. A randomized, triple blind, controlled clinical trial is conducted, in Oral and Maxillofacial Surgery Clinic. Patients were randomly allocated to three groups: I - receiving 150mg of clindamycin after surgery every 8 hours, II - receiving 300mg of clindamycin after surgery every 8 hours and III - receiving 600mg of clindamycin after surgery every 12 hours. Each group continued the therapy for five days. The investigators anticipate the overall decrease in risk of infection and other postoperative complications, however whether the differences between the clindamycin concentrations, occurrence of postoperative sequelae and pain in the three groups are statistically significant, remains to be seen. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05268835
Study type Interventional
Source Oral and Maxillofacial Surgery Clinic, Poland
Contact Anna Janas-Naze, DMD,PhD,Prof
Phone 7164485
Email anna.janas.naze@gmail.com
Status Recruiting
Phase Phase 4
Start date February 1, 2020
Completion date October 2022
View Details
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