CTRI/2017/01/007670已完成未知
A prospective,open label,two arm clinical study to evaluate the efficacy and safety of C3 Reduct ODN in the treatment of canker sore and gingivitis.
Sami Labs Limited0 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
- 未知
- 状态
- 已完成
- 发起方
- 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
入选标准
- •1 Healthy male and or female with no systemic disease.
- •2 Age between 18 to 60 years.
- •3 Having mouth ulcers with throat pain or Patients with mild to moderate gingivitis.
- •4 Patients having erupted teeth.
- •5 Willing to come for regular follow-up visits.
- •6 Able to give written informed consent.
排除标准
- •2 Presence of any systemic hematological problems.
- •3 Drug or alcohol abuse.
- •4 Under systemic or topical corticosteroid therapy.
- •5 Pregnant women or lactating mothers
- •6 History of HIV and other viral infections.
- •7 History of any antibiotic therapy in past 3 months.
- •8 History of oral prophylaxis within 6 months previous to the study
- •9 Patients with mouth breathing habit.
- •10 Patients using orthodontic and prosthodontics appliances
- •11 Are on analgesics or antiseptics.
- •12 Patients who have received any periodontal therapy in the past 6 months.
研究者
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