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临床试验/CTRI/2020/02/023395
CTRI/2020/02/023395招募中2 期

ââ?¬Å?Clinical And Histopathological Evaluation Of Ayurvedic Formulation In The Management Of Oral Submucous Fibrosis.ââ?¬?

Ministry of AYUSH0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中

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. Volunteers with diagnosed cases of oral sub mucous fibrosis clinically.
  • 2. Systemically healthy volunteers will be included.
  • 3. Patients willing to give written informed consent to participate in the study for 3 months excluding 2 weeks without drug for follow-up.

排除标准

  • 1. Persons not willing to participate in the study.
  • 2. Smokers, tobacco and/ or pan masala chewers, not ready to quit the habit.
  • 3. Persons having clinical evidence of malignant change, extension of the disease either onto the pharynx or floor of mouth.
  • 4. Pregnant and lactating women.
  • 5. Persons having systemic diseases or conditions, which can be worsened by the use of steroids.
  • 6. Persons already undergoing some OSMF treatment.
  • 7. H/o hypersensitivity to any of the control or the trial drug or any of its ingredients.
  • 8. Patients who have completed participation in any other clinical trial during the past six (06) months.
  • 9. Any other condition which the Investigator thinks may jeopardize the study.

研究者

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