Periodontitis Clinical Trial
Official title:
The Use of a Probiotic Lozenge in the Treatment of Residual Pockets After Classical Non-surgical Therapy
The aim of this study is to determine the efficacy of the usage of a probiobitc lozenge in patients with residual bleeding pockets of ≥ 5mm 3 months following scaling and rootplaning. Simultaneously the additional benefit of subgingival application of probiotics via oil drops will be investigated.
The aim of this study is to determine the efficacy of the usage of a probiobitc lozenge in
patients with residual bleeding pockets of ≥ 5mm following scaling and rootplaning.
Simultaneously the additional benefit of subgingival application of probiotics via oil drops
will be investigated.
Recruitment: This study will be a single centre (Department of Oral Health Sciences,
University Hospitals Leuven), double blind, randomized, placebo controlled clinical trial
with within each patient a split mouth design. The randomization (by means of a computer
program) and double blind design are thought to minimize the bias of the investigator and
patients.
Selection of the study population: Adults, who consult at the department of Periodontology at
the University Hospital Leuven, and who fit the inclusion criteria will be asked to
participate in this study.
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