CTRI/2023/06/054028尚未招募2 期
Clinical evaluation of Sanjivani vati and Pippaladyasava in the management of Agnimandya - a randomized parallel group study
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 with age between 18 and 60 years.
- •2.Patients having any six sign and symptoms of Agnimandya out of 10 (below
- •mentioned) along with reduced Abhyavaharan Shakti, (capacity to eat), Jarana
- •Shakti (capacity to digest), and Ruchi (appetite) for the past one week.
- •3 Udaragaurava
- •4 Shirorogaurava
- •9 Gatrasada
- •10 Malavarodha
- •3.Willing to participate in the study.
排除标准
- •1.Patients of age <18 years and >60 years.
- •2.Patients in whom Agnimandya is caused due to intake of medicine.
- •3.Patients having Tikshagni (hyper functioning of digestion and metabolic
- •activities), and Samagni (moderate Agni)
- •4.Patients having any established disease of Gastro-intestinal tracts.
- •5.Immuno-compromised states and patients with systemic infections or known cases
- •of AIDS, HIV, STD etc.
- •6.Patients with severe/history of cardiac, hepatic, cerebro-vascular disease,
- •pulmonary dysfunction, malignancy, chronic uncontrolled systemic diseases or
- •renal disorder (S. Creatinine >1.2 mg/dl) etc or poorly controlled Hypertension
- •(Blood pressure more than 160/100mm of Hg), uncontrolled Diabetes Mellitus
- •(HbA1c>=8), or any other serious medical illness.
- •7.Patients on medication with corticosteroids or any other drugs that may have an
- •influence on the outcome of the study.
- •8.History of hypersensitivity to the trial drug or any of its ingredients.
- •9.Patients who have completed participation in any other clinical trial during the
- •past three months.
- •10.Any other condition, which the Investigator thinks, may jeopardize the study.
研究者
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