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临床试验/CTRI/2025/11/097050
CTRI/2025/11/097050尚未招募2 期

A clinical study on the effect of vanapalandu in kaphaja hridroga with special reference to low left ventricular ejection fraction A proof of concept study

National Institute of Ayurveda Jaipur1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年3月20日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Change present in ejection fraction in 2D echocardiography of the heart after 2

研究概览

简要总结

A Clinical Study on the Effect of Vanapalandu in Kaphaja Hridroga with Special Reference to Low Left Ventricular Ejection Fraction: A Proof of Concept Study”

this study Aims for improvement in reduced ejection fraction of heart by giving Vanapalandu 90mg twice a day for 60 days.

outcomes are - improved ejection fraction assessing by 2D Echo by 60 days.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 59.00 Year(s)(—)
性别
All

入选标准

  • Adult patients of both genders, with stable HF (NYHA classification up to Class III and reduced EF not more than 40% and not less than 15%.
  • Patients who have already taken conventional therapy for more than or equal to 3 months and yet have the above criteria would also be included.

排除标准

  • 1.Patients with an Ejection Fraction of the Left Ventricle more than or equal to 40 percent and less than or equal to 15 percent will not be included in the study.
  • 2.Patients with a history of Unstable Angina, Acute Myocardial infarction (newly diagnosed acute cases), valvular defects, congenital heart disease, pericarditis, arrhythmia, Pericardial effusion, uncontrolled Hypertension (more than or equal to 150/90 mm Hg) 3.Patients with a history of extra Cardiac ailments like renal failure, uncontrolled diabetes mellitus (HbA1c more than or equal to 8%) with or without complications, chronic alcoholics, and pregnant/lactating women.

结局指标

主要结局

Change present in ejection fraction in 2D echocardiography of the heart after 2

时间窗: 2 months

months of trial.

时间窗: 2 months

次要结局

  • • Changes in signs and symptoms of Kaphaja Hridroga after 2 months of trial.(• Changes in symptoms using a standardized tool, the KCC Questionnaire after 2)

研究者

发起方
National Institute of Ayurveda Jaipur
申办方类型
Other [National Institute of Ayurveda Jaipur]
责任方
Principal Investigator
主要研究者

Dr Falguni Joshi

national institute of ayurveda

研究点 (1)

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