CTRI/2025/04/085568尚未招募不适用
A pre and post-trial to evaluate the effect of an Ayurveda treatment protocol in Allergic rhinitis
DrPreethi Mohan1 个研究点 分布在 1 个国家目标入组 41 人开始时间: 2025年5月3日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 41
- 试验地点
- 1
- 主要终点
- SUBJECTIVE PARAMETER
研究概览
简要总结
This study is a pre and post trial comprised od 41 samples.The treatment protocol consists of surasadi gana kashayam ,vishavilwady gutika for 14 days and amrita ghritham for 1 month.Patient will be assessed based on Total IgE,T5SS and SNOT 20 questionnaire of allergic rhinitis.The data statistically analysed by Pired t.
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
- 20.00 Year(s) 至 40.00 Year(s)（—）
- 性别
- All
入选标准
- •Those had recurrence of allergic rhinitis History of exposure to allergens Active age group of 20-40 years prone to exposure Clinical symptoms of mild allergic rhinitis and prathisyaya like rhinorrhoea, obstructed nose and sneezing.
- •Positive skin prick test for aeroallergens Mild to moderate allergic rhinitis.
排除标准
- •Asthma • DNS • ENT disorders • Food allergy • Persistent severe allergic rhinitis • Patients less than 20yrs and above 40 yrs • Pregnant ladies & lactating mothers • Patients who failed to give consent and who failed to follow –up.
结局指标
主要结局
SUBJECTIVE PARAMETER
时间窗: baseline,2weeks,6week
1. Total Nasal Symptom Scores (TNSS) Each symptom (sneezing, congestion, itching, and rhinorrhea) is graded from 0-3 by the participants during the screening and subsequent visits
时间窗: baseline,2weeks,6week
OBJECTIVE PARAMETER
时间窗: baseline,2weeks,6week
Total IgE assessment
时间窗: baseline,2weeks,6week
次要结局
未报告次要终点
研究者
Drpreethi Mohan
amrita school of ayurveda
研究点 (1)
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