CTRI/2018/08/015400尚未招募2 期
Clinical Validation of Unani Pharmacopoeal formulation Safoof e Teen in Zaheer (Dysentery)
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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 of either sex in the age group 18-65 years.
- •2. Patients of ZahÄ«r (Dysentery) having the following signs and symptoms:
- •(i) 2-8 small-volume, semiformed or unformed stools/day
- •(ii) BarÄ?z DamwÄ« (Bloody Stools) and/or BarÄ?z MukhÄ?tÄ« (Mucoid Stools)
- •(iii) E. histolytica Cysts or Trophozoites in stools
- •With or without any of the following:
- •Maghs (Tenesmus)
- •Wajaâ?? al-Batn Asfal (Lower Abdominal Pain)
- •ÄªlÄ?m al-Batn Asfal (Lower Abdominal Tenderness)
排除标准
- •1. Patients having diarrhoea with >8 stools/day
- •2. Moderate or severe dehydration
- •3. Fever (>=101 °F)
- •4. Patients having amoebic dysentery with any associated severe complications, e.g., fulminant colitis with perforation, paralytic ileus, toxic megacolon, ameboma, and liver abscess.
- •5. Clinical evidence of coexisting acute systemic illnesses
- •6. History or clinical evidence of chronic diseases requiring long-term treatment, e.g., DM, hypertension, tuberculosis, HIV infection, chronic liver disease, CKD, coeliac disease, IBD, or any other serious and/or unstable medical condition that, in the opinion of the investigator, could constitute a risk when taking study drug or could interfere with the interpretation of data.
- •7. Pregnant and lactating women
- •8. H/o Addiction (alcohol, drugs)
- •9. H/o Hypersensitivity to the study drug or any of its ingredients
研究者
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