跳至主要内容
临床试验/CTRI/2024/04/066523
CTRI/2024/04/066523尚未招募2 期

An open labelled randomised controlled clinical study To evaluate the efficacy of shunthi haridra lozengens in the management of galashundika with special reference to uvulitis - NI

Parul Institute Of Ayurved0 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
尚未招募
发起方

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 Patients from the age group of 18–40 years
  • 2 Patients having fever (below 100 degree), sore throat, cough, white spots in uvula, difficulty in breathing, chocking, thirst will be included for the present clinical trial.
  • 3 Selection will be irrespective of Gender, religion & socio- economic class.

排除标准

  • 1 Patients those who are Pregnant and lactating.
  • 2 Patient with fever above 100-degree Fahrenheit.
  • 3 Immunocompromised patients.
  • 4 Patients having uncontrolled Diabetes.

研究者

发起方
Parul Institute Of Ayurved

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