A Comparative clinical study to evaluate the efficacy of Paarthadi Kwath along with Hridbasti and calcium channel blocker on Essential Hypertension

DPU Seed Money with letter no DPU1 个研究点分布在 1 个国家目标入组 40 人开始时间: 2023年1月7日最近更新: 2023年6月15日

试验速览

阶段: 3 期
状态: 尚未招募
发起方
入组人数: 40
试验地点: 1
主要终点: Patient showing relief from clinical sign and symptoms of essential hypertension.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

A group of 20 patients will get Paarthadi Kwath along with Hridbasti for a period of 7 days. Another group of 20 patients will get Tab. Stamlo 2.5mg for 7 days. Data will be collected and compared.

研究设计

研究类型: Interventional
分配方式: Computer generated randomization
盲法: Open Label

入排标准

年龄范围: 0.00 Day(s) 至 7.00 Day(s)（—）
性别: All

入选标准

•18-70 years of either gender.
•Systolic Blood pressure less than 170mmHg more than or equal to 140mmHg.
•Distolic Blood Pressure less thann or equal to 110mmHg and more than 90mmHg.
•Hypertension Stage II according to JNC seventh report 2004.

排除标准

•Patient that past history of atrial fibrillation, acute coronary syndrome ,myocardial infarction, stroke, right ventricular hypertrophy, left ventricular hypertrophy, severe arrhythmia in last 6 months.
•Symptomatic patient with clinical feature of early heart failure.
•Secondary hypertension.
•Patient with concurrent serious hepatic dysfunction, renal dysfunction, uncontrolled pulmonary dysfunction.
•Patient suffering with diabetes nephropathy.
•Women who are pregnant, lactating or on estrogen replacement therapy.
•Alcohol and Drug abusers.
•Accelerated and maligant hypertension.

结局指标

主要结局

Patient showing relief from clinical sign and symptoms of essential hypertension.

时间窗: 0, 4 and 7 day

次要结局

To complete seven days treatment(0, 4 and 7 day)

研究者

发起方

DPU Seed Money with letter no DPU

申办方类型

Research institution and hospital

研究点 (1)

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