跳至主要内容
临床试验/CTRI/2026/01/102121
CTRI/2026/01/102121尚未招募2/3 期

A Randomised standard controlled comparative clinical study to evaluate the adjuvant effect of Sarpagandha Mishrana along with conventional anti hypertensive therapy in the management of essential hypertension

未提供1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2026年3月1日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
44
试验地点
1

研究概览

简要总结

This study is a randomized standard controlled comparative clinical study to evaluate the adjuvant effect of Sarpagandha Mishrana along with conventional anti-hypertensive therapy in the managemnt  of Essential Hypertension, that will be conducted in BLDEAS AVS Ayurveda Mahavidyala Hospital and Research  Vijayapura 586109  Karnataka India

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 79.00 Year(s)(—)
性别
All

入选标准

  • 1.Patient taking Amlodipine but not achieving desired results are included.
  • 2.Patients diagnosed as Essential Hypertension as per diagnostic criteria.
  • 3.Subjects willing and able to participate in the study.

排除标准

  • 1.Secondary Hypertension.
  • 2.Patients with a prior diagnosis of severe or malignant hypertension, moderate hypertension associated with complications, cerebrovascular disorders, coronary artery diseases, kidney conditions, heart failure, cardiomyopathy, pre-eclampsia or eclampsia, diabetes mellitus, retinopathy, or any other coexisting physical or mental health condition.

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Dr Biradar Varsha Ravikumar

BLDEAS AVS Mahavidyala Hospital and research center

研究点 (1)

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