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临床试验/IRCT20210821052241N1
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

Esfahan University of Medical Sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:

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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