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临床试验/CTRI/2012/09/003020
CTRI/2012/09/003020已完成未知

An open labeled clinical trial to evaluate the efficacy and safety of â??Hypercumâ?? for the treatment of hypertension and associated complications

MS Natural Solutions0 个研究点目标入组 16 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
16

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

  • Males and females of age group 18-60 years
  • Subjects who are willing to give written informed consent
  • Patient running with Anti Hypertensive drugs or patient having known to be a Hypertensive patient but not yet approached any system of medication.
  • Diabetic Patient or Patient running with Renal Failure or Patient having Metabolic Syndrome
  • Female subjects who are confirmed as non-pregnant status and agree to comply with proper contraception throughout the study duration
  • Patient is willing and able to comply with all trial requirements

排除标准

  • Severe essential hypertension
  • Significant renal insufficiency [Serum Creatinine > 159 µmol/L ( > 1.8 mg/dl)]
  • History of cerebro-vascular disease
  • Patients with a history of HIV infection, AIDS, hepatitis B or C, or other immunosuppressive disorders
  • Current diagnosis or a history of malignancy
  • Drug of abuse within the past 2 years
  • Pregnancy or breastfeeding
  • Present history of mental diseases
  • Previous participation in a clinical trial within 6 months

研究者

发起方
MS Natural Solutions

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