跳至主要内容
临床试验/CTRI/2024/05/068028
CTRI/2024/05/068028尚未招募2 期

Single centric non-randomized open clinical trial phase II in Swasakasam (Bronchial asthma) with siddha medicine Sangkaara vairavan among patients attending OPD at Government siddha medical college hospital, Chennai

Dr R Sasirekha1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年9月2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
40
试验地点
1
主要终点
The Outcome will be assessed by reduction in clinical symptoms like wheeze, dyspnea and chest tightness

研究概览

简要总结

Bronchial asthma is an important public health problem at the global level. It is a chronic reversible inflammatory destructive disease of the airways characterized by recurrent paroxysmal attacks of dyspnea chiefly expiratory in nature accompanied by wheeze which may subside spontaneously or with treatment. There are complex and confounding associations and relationships with infections and infestations, air pollution, tobacco smoking and environmental tobacco smoke exposure. According to a global asthma report among India’s 1.31 billion people, about 6% of children and 2% of adults have asthma. In India, statistical data shows that 0.92%of women and 3.04% of men were suffering from asthma.

Thus, in Siddha system of Medicine, there are unique combination of medicines, which have solution to the present scenario of Bronchial asthma. One such combination is SANGKAARA VAIRAVAN which will be cost effective and reliable. The method of preparation of the medicine is easy and the raw drugs are also easily available.

The aim of the study is the management of SWASAKASAM (BRONCHIAL ASTHAMA) with siddha medicine SANGKAARA VAIRAVAN  and the objective is to determine the therapeutic efficacy and safety profile of the siddha medicine SANGKAARA VAIRAVAN  in the management of SWASAKASAM (BRONCHIAL ASTHAMA). As the literary evidences support the usage of medicine, in the disease, hypothesis is created such a way that the efficacy of SANGKAARA VAIRAVAN will be a better solution for SWASAKASAM (BRONCHIAL ASTHAMA).

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 60.00 Year(s)(—)
性别
All

入选标准

  • Cough with tenacious sputum Dyspnea H/O Wheeze or without wheeze Chest tightness Peak expiratory flow rate between 60-80%.

排除标准

  • K/C/O Chronic bronchitis K/C/O Bronchiectasis K/C/O Pulmonary TB K/C/O Congestive cardiac failure K/C/O Status asthmaticus Pregnancy and lactating mothers.

结局指标

主要结局

The Outcome will be assessed by reduction in clinical symptoms like wheeze, dyspnea and chest tightness

时间窗: 48 days

次要结局

  • assessing peak expiratory flow rate from moderate persistent (60-80%) to mild persistent & mild intermittent (≥80%)(48 days)

研究者

发起方
Dr R Sasirekha
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr R Sasirekha

Government siddha medical college

研究点 (1)

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