CTRI/2025/03/082008尚未招募2 期
COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OF BRIHAT VASAVLEHA AND SHADBINDU TAIL NASYA IN THE MANAGEMENT OF PRANAVAHA SROTO DUSHTI W.S.R. OF RESPIRATORY ALLERGIC DISORDERS IN CHILDREN
Madan Mohan Malviya Government Ayurved College Udaipur1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年3月17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
- 60
- 试验地点
- 1
- 主要终点
- to check the effectiveness and efficacy of the drug and procedure in Respiratory Allergic Disorders
研究概览
简要总结
This study is conducted on upper respiratory tract infections on 60 cases through brihat vasavleh and shadbindu tail nasya . To conduct the study two groups will be there
group A - brihat vasavleh and shadbindu tail nasya
group B- placebo and shadbindu tail nasya
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- None
入排标准
- 年龄范围
- 6.00 Year(s) 至 14.00 Year(s)（—）
- 性别
- All
入选标准
- •Children whose parents are willing to give consent/assent for clinical trial.
- •Children having cardinal features of respiratory allergy.
- •Children with a history of three or more episode within the past year.
排除标准
- •Children cases of respiratory allergies that are severe and complicated.
- •Children aged below 06 years and above 14 years of either sex.
- •Children suffering from major systemic illness necessitating long-term treatment.
- •Children with evidence of malignancy, genetic or congenital anomaly.
- •Children diagnosed with Tuberculosis, Plural effusion, Emphysema, Lung abscess, Bronchiectasis, Pleurisy, Nasal polyps etc.
- •H/o hypersensitivity to any of the trial drug or their ingredient.
结局指标
主要结局
to check the effectiveness and efficacy of the drug and procedure in Respiratory Allergic Disorders
时间窗: 56 days
次要结局
- To compare both the drugs(56 days)
研究者
Dr Nazneen
Madan Mohan Malviya Government Ayurved College Udaipur,
研究点 (1)
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