CTRI/2017/05/008535已完成未知
Control of Glycemic Variability using a polyherbal: A randomized placebo controlled study of whole herb formulations.
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 50
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
- •Adult males and non-pregnant females aged >=18 years having a diagnosis of pre-diabetes (impaired fasting glucose or impaired glucose tolerance) or diabetes and meeting one of the following criteria
- •1.Fasting Plasma Glucose >=100 mg/dL, fasting defined as no caloric intake for at least 8 hours, AND
- •2.Glycosylated haemoglobin (A1C) >= 6 %. The test should be performed in a laboratory using a method that is NABL certified and standardized within last 3 months.
排除标准
- •Any one of the following
- •1.Patients on Insulin therapy.
- •2.Any history suggestive of micro vascular or macro vascular disease â?? coronary artery disease, stroke, peripheral artery disease or diabetes related retinal changes.
- •3.Women in child bearing age unable to practice any form of contraception
- •4.Patients with diagnosis of Anemia (Hb <11 g/dl in Female and <13 g/dl in Male)
- •5.Impaired renal function; eGFR <60mls/min/1.73m2.
- •6.Known history of any chronic illness taking regular pharmacological agents.
- •7.Blood pressure fluctuations exceeding 20mmHg on 2 subsequent clinic visits or known history of hypotension or bradycardia in last 6 months or taking 3 or more antihypertensive medications regularly in the last 6 weeks
- •8.Known history of autonomic dysfunction like diabetic autonomic neural imbalance or neuropathy
- •9.Current or former employees of organic India or any potential conflict of interest in participation
- •10.Participating in another clinical trial with an active intervention or drug or device with last dose taken within 60 days.
- •11.Refusing consent or physician uncomfortable with patient compliance to treatments or follow up.
研究者
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