Evaluation of efficacy of Rajrasayan verses Vachadi Avaleha in the Management of Pratishyaya (Rhinitis) in School going Children : A Randomized Controlled Trial
试验速览
- 阶段
- Phase 3 4
- 状态
- 尚未招募
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- To assess the reduction in the symptoms of pratishyaya on the basis of subjective and objective criteria.
研究概览
简要总结
The volunteers will be informed about the study protocol. Willing participants will be randomly
selected as per computer-generated table. The clinical research format will be prepared
and validated.Before the study approval will be taken from IEC, MGACHRC, Salod (H) Wardha, and CTRI
registration will be done. After selection, each participant will be tested individually and selected
according to selection criteria. They are divided into two groups. The trial is a Randomized Single blind clinical control trial.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 4.00 Year(s) 至 18.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients suffering from Pratishaya less than 3-4 days Patients in the age group of 4 year to 18 years will be selected irrespective of sex, socio-economic status and religion Children whose parents are giving written consent for their child to participate in the study.
排除标准
- •Mucoid and purulent or blood-stained nasal discharge Patient suffering from nasal polyps, Deviated nasal septum Any other systemic illness for eg.
- •Fever Rhinitis associated with immunodeficiency like HIV.
结局指标
主要结局
To assess the reduction in the symptoms of pratishyaya on the basis of subjective and objective criteria.
时间窗: Treatment for 7 days and post treatment follow up on 14th and 21st day.
次要结局
- To assses the recurrence of pratishyaya in school going children.(Follow up on 14th & 21st day.)
研究者
DR PRIYANKA PRASHANT MUNJEWAR
Mahatma Gandhi Ayurved College, Hospital and Research Centre Salod(H) Wardha