Comparison of antiplaque efficacy of a commercially available toothpowder and toothpaste in young adults: A single blind randomized controlled equivalence trial

Amrita School of Dentistry0 个研究点目标入组 89 人开始时间: 待定最近更新: 2021年11月24日

试验速览

暂无简介。

•1. Subjects aged 18-25 years
•2. Subjects with no systemic disorders like diabetes and hematological disorders
•3. Subjects with atleast 20 natural teeth
•4. Patients with gingivitis (moderate and severe)
•5. No history of periodontal therapy
•6. No history of use of antibiotics within preceding 6 months of start of study
•7. Subjects who give a voluntary informed consent to participate in the study

•1. Known allergy to constituents of the formulation of toothpowder and toothpaste
•2. Patients undergoing orthodontic treatment
•3. Advanced periodontal disease (purulent exudate, tooth mobility, and/or extensive loss of periodontal attachment or alveolar bone)
•4. Pregnant women or women who are breast-feeding
•5. Those whose received a dental prophylaxis in the past two weeks prior to baseline examinations.
•6. Smokers

发起方

Amrita School of Dentistry