CTRI/2018/06/014383已完成1 期
A comparative study of the effect of Chhinnavahni Kashaya Vati along with Agnimantha Kwatha and Metformin in the management of Madhumeha w.s.r. to Diabetes Mellitus (Type-II)
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 60
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 aged between 20 to 60 years.
- •2.If yes in any two of the four:
- •a)Blood sugar â??fasting > 126 and <= 250 mg/dl.
- •b)PP > 200 mg/dl and <=350 mg/dl.
- •c)Glycosylated Haemoglobin (HbA1c) > 6.5% and < 9%.
- •d)Subjects having classical symptoms of diabetes with random glucose levels >=200mg/dl (<=350mg/dl).
- •3.Diagnosed cases of Type II Diabetics having Glycosylated Haemoglobin (HbA1c) between 6.5-9% without or {with metformin in a dose1g-1.5g/day (for Group-B)}.
- •4. Subjects who are able to come for follow up on fixed visits and are well aware about the treatment plan.
- •5.Subjects willing to participate and able to provide written informed consent.
排除标准
- •1.Age below 20 and above 60yrs.
- •2.Subject of Type-I DM (insulin dependent DM) or Type-II DM on insulin/OHAâ??s other than metformin/ any other AYUSH medication for glucose control.
- •3.Subjects suffering from the complications of Diabetes mellitus viz., diabetic neuropathy, diabetic nephropathy, diabetic retinopathy etc. which require an urgent treatment.
- •4.Uncontrolled Hypertensive subjects (BP with or without medication >140/90 mmHg after 5 mins of rest).
- •5.Subjects with any unstable Heart disease or known cases of MI, unstable angina or CHF.
- •6.Patients with concurrent Hepatic Dysfunction (defined as AST and/or ALT > 2 times of the upper normal limit) or Renal Dysfunction, uncontrolled Pulmonary Dysfunction (asthmatic and COPD subjects).
- •7.Subjects with current or past diagnosis of malignancy (any malignancy diagnosis in last five years).
- •8.Subjects who have a recent history or who are currently known to abuse of alcohol or drugs.
- •9.Subjects suffering from major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Psycho-Neuro-Endocrinal disorders, TB, AIDS etc).
- •10.Female subject of child bearing potential who do not agree to remain abstinent or use medically acceptable methods of contraception during the study therapy and for 4 weeks after the end of study therapy.
- •11.Pregnant / Lactating women.
- •12.Subject on systemic or oral steroids, oral contraceptive pills or estrogen replacement therapy.
- •13.Subjects having hypersensitivity to any of the trial drug.
- •14.Subjects who have completed participation in any other clinical trial during the past six (06) months.
研究者
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