CTRI/2022/03/040721已完成2 期
CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OFCORDYCEPS POWDER (CORDYCEPS SINENSIS) AS A NUTRITIONALSUPPLEMENT IN PATIENTS WITH CO MORBIDITIES
DXN Manufacturing India Pvt Ltd0 个研究点目标入组 24 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 24
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. Participants aged 18-60 years (both sex).
- •2. Participants who are presenting with any one of the co morbidities like
- •Systemic hypertension or Diabetes Mellitus or Hyperlipidemia
排除标准
- •1. Participants presenting with fever and acute infections, will be excluded.
- •2. History of heart, liver or kidney failure.
- •3. Allergy or intolerance to the individual constituents in test product.
- •4. Patients with history of abnormal thyroid
- •5. Patients with history of any malignancy.
- •6. History of any Neurodegenerative disease
- •7. Organ transplantation
- •8. Allergy to fungi
- •9. Subjects who are pregnant and lactating mothers, or with any serious
- •disease condition limiting full adhesion to the protocol.
- •10. Participation in an investigational drug trial in the 30 days prior to the
- •screening visit.
研究者
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