Comparison study, identifying statisticial differences in biofilm removal and gingival inflamation markers based upon the cleaning efficacy of interdental oral irrigation and interdental brushes in adults with gingivitis

Sydney Dental Hospital0 个研究点目标入组 40 人开始时间: 2021年12月9日最近更新: 2021年12月13日

适应症

试验速览

暂无简介。

•1. Oral Disease status/ or disease group for study: Embrasure space of 2 or 3. PSR code<=3.
•2. Gender: no restrictions
•3. Age range: >18 years
•4. At least 24 natural teeth
•5.Willingness to provide informed consent and willingness to participate and comply with the study requirements.

•1. Women lactating, pregnant or of childbearing potential who are not willing to avoid becoming pregnant during the study.
•2.Participants with a history of active periodontal disease with a PSR code of 4.
•3.Participants with a history of diabetes, tobacco smoking, xerostomia (dry mouth), any form of chronic inflammatory disease.
•4.Participants who have taken antibiotics within the past six weeks.
•5.Participants currently experiencing psychological illness or other conditions which may interfere with their ability to understand the study requirements or interfere with their motivation to participate in the study, or the evaluation of the study outcome.
•6.As the following medication(s) can have interactive effects and may interfere with the participant’s ability to meet the study requirements, they cannot be administered during the clinical study (anticoagulants, anti-convulsant, immunosuppressants, tricyclic antidepressants)
•7. Participants that have a medical condition which inhibits their ability to safely use the OH tools, e.g. multiple sclerosis, Parkinson’s disease.

发起方

Sydney Dental Hospital