CTRI/2019/05/019452已完成2 期
A Randomized, multi-center, Open labeled, Comparative, Prospective Clinical Study To Evaluate Efficacy and Safety of Yesaka Liquid as an Add-on therapy to Oral Hypoglycemic Agent (OHA) in Type 2 Diabetic Patients. - NI
Simandhar Herbal Pvt Ltd0 个研究点目标入组 0 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
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.Subjects suffering from Type 2 Diabetes Mellitus for more than one year, and stabilized on mono/ polydrug anti-diabetic therapy for at least last 3 months.
- •2.Subjects having HbA1C value 7-11% (both inclusive) at screening.
- •3.Subjects having Fasting Plasma Glucose between 126 -252 mg/dl (both inclusive) at screening.
- •4.Subjectâ??s ECG not demonstrating any signs of uncontrolled arrhythmia / acute ischemia and X- ray chest not showing any active lesion of tuberculosis.
- •5.A urine pregnancy test is required for all female subjects unless subject has had a hysterectomy, tubal ligation, or is > 2 years post menopause.
- •6.Subjects willing to follow the procedures as per the study protocol and voluntarily signing informed consent form
排除标准
- •1.Subjects on insulin therapy.
- •2.Subjects suffering from type-1 DM or types of Diabetes mellitus other than Type-2
- •3.Subjects with known history of chronic hepatic or renal disease.
- •4.Subjects with known history of active malignancy.
- •5.Subjects with known history of significant cardiovascular event 12 weeks prior to randomization.
- •6.Subjects with known history of major complications of Diabetes like Ketoacidosis, Nephropathy, Neuropathy, Retinopathy, and Diabetic wounds.
- •7.Subjects with known history of chronic, contagious infectious disease, such as active tuberculosis, Hepatitis B or C, or HIV.
- •8.Subjects with known history of active metabolic or gastrointestinal diseases that may interfere with nutrient absorption, metabolism, or excretion, excluding diabetes.
- •9.History of Use of any other investigational drug within 1 month prior to randomization
- •10.Known history of hypersensitivity to ingredients used in study drug
- •11.Pregnant and Lactating females.
- •12.Any other conditions which in the opinion of investigator will place the subject at risk or will influence the conduct of study or interpretation of results
研究者
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