MTZ Plus AMX in the Treatment of Smokers and Non-smokers

Sample size calculation:

This study is designed to compare the clinical and microbiological effects of the treatment of smoker and non-smoker subjects with SRP+MTZ+AMX. The ideal sample size to assure adequate power for this clinical trial was calculated considering differences of at least 1mm between groups for clinical attachment level (CAL) in initially deep periodontal sites (PD ≥ 7 mm). It was also determined that the standard deviation of CAL change at deep sites would be 1.0 mm based on our earlier studies of smokers and non-smokers receiving SRP combined with MTZ+AMX. Based on these calculations, it was defined that 26 subjects per group would be necessary to provide an 85% power with an α of 0.01. Considering an attrition of about 20%, it was established that at least 32 subjects should be included in each treatment group.

Experimental design and treatment protocol:

In this cohort clinical trial, subjects will be assigned according to their smoking status, into smoker and non-smoker groups. All subjects will receive SRP combined with systemic MTZ (400 mg) and AMX (500 mg). Both antibiotics will be administered T.I.D. for 14 days. Before the study begins, all subjects will receive full-mouth supragingival scaling and instruction on proper home-care techniques. They will receive the same dentifrice to use during the study period (Colgate Total). All subjects will receive full-mouth SRP performed under local anesthesia in four to six appointments lasting approximately 1h each. Treatment of the entire oral cavity will be done in 14 days. SRP will be performed by one trained periodontist using manual instruments. The antibiotic therapies will start immediately after the first session of mechanical instrumentation. The University Pharmacy will prepare the antibiotic pills and send them to the study coordinator, who will mark the code number of each subject on a set of two packs and give them to the examiner. All subjects will receive clinical and microbiological monitoring at baseline and at 3, 6 and 12 months post-therapy.

Clinical monitoring:

One calibrated examiner will perform clinical monitoring and the treatment will carried out by another clinician. Thus, the examiner and the clinician will be masked as to the nature of the treatment groups. Visible plaque (presence or absence), gingival bleeding (presence or absence), bleeding on probing (BOP; presence or absence), suppuration (presence or absence), PD (mm) and clinical attachment level (CAL, mm) will be measured at six sites per tooth (mesiobuccal, buccal, distobuccal, distolingual, lingual and mesiolingual) in all teeth, excluding third molars. The PD and CAL measurements will be recorded to the nearest millimeter using a North Carolina periodontal probe.

Microbiological Monitoring:

Subgingival plaque samples will be collected at baseline and at 3, 6 and 12 months post-SRP from nine non-contiguous interproximal sites per subject. The select sites will be randomized in different quadrants and subset according to baseline PD, three samples in each of the following categories: shallow (PD<3 mm), intermediate (PD 4-6 mm) and deep (PD>7 mm). After the clinical parameters have been recorded, the supragingival plaque will be removed and the subgingival samples will be taken with individual sterile curettes (Gracey #11-12) and immediately placed in separate Eppendorf tubes containing 0.15 ml of buffer (TE). One hundred microliters of 0.5 M sodium hydroxide (NaOH) will be added to each tube and the samples will be dispersed using a vortex mixer. The samples will be analyzed by Checkerboard DNA-DNA hybridization.