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临床试验/CTRI/2020/02/023517
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.

All India Institute of Ayurveda0 个研究点目标入组 30 人开始时间: 待定最近更新:

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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