IRCT20210821052241N1招募中3 期
Evaluation of clinical effects of two probiotic products, Lactogum & ParsiLact-LA on oral health of patients treated with removable and fixed orthodontic appliances
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- no limit 至 no limit(—)
- 性别
- All
入选标准
- •Patients planned for removable functional orthodontic appliances or full arch both jaws fixed orthodontic appliance therapy.
- •Good general health.
- •Good oral health (have a dental history that includes brushing at least once a day).
- •Be willing and able to comply with the trial regime.
- •To have normal tooth anatomy, oral mucosa and periodontal status.
排除标准
- •Inability to obtain informed consent.
- •Presence of allergies, food sensitivities or food intolerance.
- •Any congenital syndromes of the head and neck.
- •Medical contraindications such as heart conditions or Gastrointestinal disorders.
- •Any state or diseases necessitating taking immunosuppressants or antibiotics or any medication chronically prior to the procedures.
- •Any special physical or mental needs that would compromise patient cooperation.
- •History of surgery within the past year or planned to have a surgery in the next 90 days.
- •Severe fever, nausea, vomiting, bloody Diarrhea or severe abdominal pain within the past 1 month.
- •Chronic use of probiotics or food supplements of any kind and use of antibiotics, steroids, hormones, oral prophylaxis or anti-microbial mouth wash or tooth paste within 1 month before the start of the study.
- •Use of products containing xylitol and fluoride or other anti cariogenic products.
- •Poor compliance with oral hygiene regimens; poor periodontal health(presence of calculus and/or periodontal pocket); extensive dental restorations or uncontrolled caries activity.
研究者
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