CTRI/2017/04/008386
已完成
3 期
Evaluation of efficacy and safety of â??AHPL/AYTOP/2014Aâ?? in patients suffering from aphthous ulcers - an open label, randomized, multi-center, prospective, active controlled, parallel group, clinical study. - NI
Ari Healthcare Pvt Ltd0 个研究点目标入组 0 人待定
概览
- 阶段
- 3 期
- 干预措施
- 未指定
- 疾病 / 适应症
- 未指定
- 发起方
- Ari Healthcare Pvt Ltd
- 状态
- 已完成
- 最后更新
- 4年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •1\.Patients clinically diagnosed as aphthous ulcers
- •2\.Minor Mouth ulcers that have appeared less than a week prior to the enrollment
- •3\.Ulcers at accessible locations (labial, buccal mucosa, tongue preferably)
- •4\.Who can make all necessary visits and comply with the study procedures
- •5\.Subject willing to participate in clinical trial and who have read, understood and signed informed consent form
排除标准
- •1\.Subjects Suffering from any other oral or dental disease or active skin disease.
- •2\.Patient under treatment of ulcers with systemic steroids, vitamins, antibiotics, antihistamines, oral Retinoids or immunomodulatory agents within three months before study entry.
- •3\.Patients having any major systemic diseases including genetic, endocrinal diseases, cancer, HIV, AIDS
- •4\.Known cases of hematological disorders, ulcerative colitis or Crohns disease.
- •5\.Patient who had a history of probable sensitivity to any mouthwash or toothpaste
- •6\.Patients having Anemia or known iron, folic acid, Vit. B12 deficiency
- •7\.Patient having addiction of alcohol or smoking or tobacco chewing
- •8\.Pregnant or lactating women
- •9\.Patients having known hypersensitivity to ingredients used in the study drugs
结局指标
主要结局
未指定
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