CTRI/2020/02/023517已完成2 期
The efficacy of Shatyadhi churna in the management of vataja pratisyaya (allergic rhinitis) in children- A randomized controlled clinical trial.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. Age group 6 to 16 years irrespective of their sex.
- •2. Patients having following 4 or more diagnostic symptoms of vatajapratishaya ie.
- •a)Kshavathu(sneezing),
- •b)nasa srava(rhinorrhea),
- •c)Nasauparodha(nasa blockage) ,
- •d)mukha shosha(dry mouth) ,
- •e)sirasoola(headache) ,
- •f)nasa –bru kandu(itchy nose –eyebrow)
- •-for a minimum of one year immediately preceding the study Screening Visit.
- •A minimum score of 4 on Vataja pratisyaya severity score index will be included in the study.
- •3. Gives written informed consent (parent/legal guardian) and assent (from the child), including privacy authorization as well as adherence to concomitant medication withholding periods, prior to participation.
排除标准
- •1.Age under 6 years and above 16 years irrespective of sex.
- •2.Patients having lower respiratory tract infection.
- •3.Upper Respiratory complaints such as Nasal polyposis, Nasal tumours.
- •4.Patients with adenotonsillar hypertrophy, craniofacial syndromes, or neuromuscular diseases.
- •5.Patients with history of nasal surgery.
- •6.Other respiratory infectious conditions such as Tuberculosis, Plural effusion, Emphysema, Lung abscess, Bronchiectasis, pneumonia, Pleurisy.
- •7.Congenital anomalies of respiratory tract or rhinitis due to trauma.
- •8.Patients suffering from chronic debilitating diseases like JDM, HIV, HBsAg, immune compromised children etc.
- •9.Patients who are not willing to be included in the study protocol and also who are not willing to give the consent for the study.
研究者
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