CTRI/2019/05/019339已完成1 期
Preclinical and clinical evaluation of safety and efficacy of Pramehakulantaka Rasa in the management of Madhumeha w.s.r. to Diabetes Mellitus TypeII
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 64
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 ready to give concern for the trial & willing to participate in the study for 3 months.
- •2.Patients between the age group of 31-70 years in either sex.
- •3.Newly diagnosed & confirmed cases of Mahdumeha (Type II Diabetes Mellitus) not talking allopathic drug or Insulin Therapy.
- •4.Patients with Fasting Blood Sugar (FBS) in the range of 126mg/dl â?? 250mg/dl or Post Prandial Blood Sugar (PPBS) in the range of 200mg/dl â?? 300 mg/dl and Glycosylated Haemoglobin (HbA1c) 6.5% - 9.0%.
- •5.Presence of Cardinal symptoms of Diabetes Mellitus eg. (3P- polyuria, polydipsia, polyphagia).
排除标准
- •1.Patients below 31years of age & above 70 years of age.
- •2.Patients having Type I DM.
- •3.F.B.S. > 250 mg/dl and P.P.B.S. > 300 mg/dl.
- •4.Patients of Type II DM who are on insulin therapy and Drug induced DM.
- •5.Patients on allopathic anti-diabetic drug.
- •6.DM with complications and Madhumeha with ashadhya upadrava.
- •7.Patients having any serious illness like cardiovascular diseases, renal diseases, hepatic diseases, malignancy, any other endocrinopathies etc.
- •8.Pregnant and lactating mother.
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