Comparison of Patient Perceptions and Practitioner Preferences in Guided Biofilm Therapy Versus Ultrasonic Piezo Scaling: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Plaque index and questionnaires assessing comfort, pain, sensitivity, efficiency, and satisfaction levels ranges from 0-10 after treatment
研究概览
简要总结
Periodontal diseases, primarily caused by microbial biofilm, remain one of the most prevalent oral health problems and a major reason for tooth loss in adults. Although conventional scaling and root planing (SRP) with hand and ultrasonic instruments has long been considered the gold standard for biofilm removal, it is often time-consuming. technique-sensitive, and associated with adverse effects such as cementum loss. postoperative sensitivity, and considerable patient discomfort. These limitations highlight the need for less invasive, more efficient, and patient-friendly alternatives. Guided Biofilm Therapy (GBT), which integrates air-polishing with ultrasonic instrumentation, offers a systematic and minimally invasive approach that may reduce treatment time, enhance patient comfort, and improve clinical efficiency while maintaining therapeutic effectiveness. Therefore, it is necessary to evaluate and compare GBT with conventional scaling to determine its clinical relevance, patient acceptance, and practitioner preference.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •Participants eligible for the study were adults aged 18 to 60 years with a minimum of 20 natural teeth.
- •The teeth included in the study were required to be free from dental caries, abrasion, erosion, or any other structural defects.
- •Only systemically healthy individuals diagnosed with Stage I or Stage II periodontitis were included.
- •Additionally, participants were required to have no caries or abrasions present in the teeth selected for evaluation.
排除标准
- •The exclusion criteria included individuals with systemic diseases such as diabetes, heart disease, or cancer, and those suffering from respiratory diseases including chronic obstructive pulmonary disease or asthma.
- •Participants who had used antibiotics within three months prior to the start of the study were also excluded.
- •In addition, pregnant or lactating women, individuals with a known allergy to chlorhexidine or erythritol, and smokers consuming more than 10 cigarettes per day were not eligible for inclusion.
- •Furthermore, individuals who were unwilling to undergo the proposed treatment were excluded from the study.
结局指标
主要结局
Plaque index and questionnaires assessing comfort, pain, sensitivity, efficiency, and satisfaction levels ranges from 0-10 after treatment
时间窗: BASELINE
次要结局
未报告次要终点
研究者
Dr Kata Sai Sruthi
GSL DENTAL COLLEGE AND HOSPITAL
