Effect of Three Periodontal Therapies in Current Smokers and Non-Smokers
Periodontitis, Periodontal Diseases
About this trial
This is an interventional treatment trial for Periodontitis
Eligibility Criteria
Inclusion Criteria: > 20 teeth > 5% sites (approx. 8 sites) with pocket depth > 4 mm and / or 5% sites with attachment level > 4 mm and mean AL < 4.5 mm and mean PD < 3.9 mm (not including tooth brush abrasions). Exclusion Criteria: > 50% of sites with pocket depth or attachment level > 4 mm Pregnancy or nursing Periodontal or antibiotic therapy in the previous 6 months Any systemic condition which might influence the course of periodontal disease or treatment (e.g. diabetes, AIDS) Any systemic condition which requires antibiotic coverage for routine periodontal procedures (e.g. heart conditions, joint replacements etc.) Liver disease Any known allergy to amoxicillin, metronidazole or doxycycline Lactose intolerance
Sites / Locations
- Department of Periodontology
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Active Comparator
Active Comparator
Scaling and root planing alone
SRP + Metronidazole
SRP + MET + Amoxicillin + Doxycycline
Full mouth scaling and root planing (SRP) alone plus a placebo pill taken twice daily for 2 weeks.
Full mouth Scaling and Root Planing plus Metronidazole (MET) 250 mg tid x 14 days
Full mouth Scaling and Root Planing plus Metronidazole (MET) 250 mg tid x 14 d and Amoxicillin (AMOX) 500 mg tid for 14 days and local drug delivery of Doxycycline (TET LDD) in pockets >4mm