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临床试验/CTRI/2008/091/000053
CTRI/2008/091/000053尚未招募2 期

A Proof of Concept prospective, double blind, placebo controlled randomised, multi¬centric study to evaluate the activity and safety of PHP Diabetes in patients freshly diagnosed with Type 2 Diabetes mellitus

Council of Scientific & Industrial Research, New Delhi0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
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

  • Patients satisfying all the following criteria are included in the study:
  • 1.Patients of either sex between the age group 18 to 60 years (both inclusive).
  • 2.Patients who are freshly diagnosed as suffering from Type 2 Diabetes mellitus not on any oral hypoglycemic agent.
  • 3.Patients with HbA1c between 7.0-9.5 %.
  • 4.Patients ready to abide by trial procedures and to give informed consent.

排除标准

  • A.1. Patients suffering from any of the following conditions will be excluded from the study:
  • a.Type 1 diabetes mellitus
  • b.Patients with severe hyperglycemia (FBS >234 mg% or PPBS > 360 mg%)
  • c.Patients with fasting serum cholesterol >260mg% and serum Triglycerides>300 mg%.
  • d.Patients with HbA1c more than 9.5 %.
  • e.Patients with ASAT and ALT levels greater than 2.5 times the upper normal limits
  • f.Severe renal, hepatic or respiratory disorder.
  • g.Patients with psychiatric disorder.
  • h.Patients with haematological disorders
  • i.History of smoking (more than 10 cigarettes/day) or alcohol intake > 20 gm/day.
  • j.Complications of diabetes such as
  • Proliferative type retinopathy
  • Nephropathy with laboratory values greater than 1.5 times the upper normal limits
  • Presence of ketone bodies in urine analysis
  • Ischemic heart disease with any cardiac event in last 6 months
  • Fasting serum cholesterol >260mg. % and serum Triglycerides >300 mg%.
  • 2.Patients with BMI >35 kg/m2
  • 3.Patients who are likely to undergo surgery during the study period.
  • 4.Patients who have participated in any investigational study in the last 4 weeks.
  • 5.Patients having known hypersensitivity to the study drugs.
  • 6.Patients with any severe infection
  • 7.Patients with a history of intake of ANY Ayurvedic/herbal/homeopathic/dietary supplements (including Vitamin E) or any alternative therapies in the last one month
  • B. Pregnant or lactating females and women in child bearing age refusing to use contraceptives.

研究者

发起方
Council of Scientific & Industrial Research, New Delhi

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