CTRI/2015/01/005473招募中2 期
Clinical Evaluation of Parthadyarishta (Arjunarishta) and Sarpagandha Vati in the management of Essential Hypertension (Uccha Raktachap)
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 76
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. Diagnosed patients of essential hypertension S.B.P. >= 140 Hg. and_ < 159 Hg.D.B.P. _ > 90 Hg. and _ < 99 Hg mm Hg (Hypertension Stage-1,as per J N C VII report,2004)
- •2. Willing and able to participate for 14 weeks
排除标准
- •1. Known clinical diagnosed cases of coronary diseases
- •2. Patients who have a past history of Atrial Fibrillation, Acute Coronary Syndrome, Myocardial Infarction, Stroke or Severe Arrhythmia in the last 6 months.
- •3. Symptomatic patients with clinical evidence of Heart failure.
- •4. Secondary hypertension.
- •5 Patients with concurrent serious Hepatic Dysfunction (defined as AST and/or ALT >3 times of the upper normal limit) or Renal Dysfunction (defined as S. creatinine >1.2mg/dl, uncontrolled Pulmonary Dysfunction(asthmatic and COPD patients) or other concurrent severe disease.
- •6.Patients with Diabetes Mellitus {B.S. (F) > 126 mg/dl and / or B.S. (2 hr. PP) >200 mg/dl}
- •7. Women who are pregnant or lactating.
- •8. Patients on steroids, oral contraceptive pills or estrogen replacement therapy.
- •9. Alcoholics and/or drug abusers.
- •10.Serum Triglycerides >= 250 mg/dl
- •11.Patients with evidence of malignancy
- •12. Patients suffering from major systemic illness necessitating long term drug treatment (Rheumatoid arthritis, Psycho-Neuro-Endocrinal disorders, etc.)
- •13. H/o hypersensitivity to any of the trial drugs or their ingredients.
- •14. Patients who have completed participation in any other clinical trial during the past six (06) months.
- •15. Any other condition which the Investigator thinks may jeopardize the study.
研究者
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