A Randomised Controlled Clinical Study To Evaluate The Efficacy Of Pippali Choorna Modified Into Lozenges In The Management Of Tundikeri In Children
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- 1.Assessment will be made on the basis of improvement in the clinical features.
研究概览
简要总结
This study is randomized, parallel group, actively controlled clinical study with comparative standard
study- Peetha saireyaka lozenges and interventional drug- Pippali choorna modified into lozenges with the dosage of 6gm after food TID in divided doses. The study is conducting on patients of Tundikeri belongs to age of
7years to 15years who gives written and verbal by parents for undergoing clinical Study. Study will
be conducting in Alvas Ayurveda Medical College And Hospital, Vidyagiri, Moodabidri.
Interventional period of this study is 21 days assessment will be done on before treatment, 2nd day, 5th day,
7th day and 21st day.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 7.00 Year(s) 至 15.00 Year(s)（—）
- 性别
- All
入选标准
- •1.Patients of either gender aged between 07 to 15 years.
- •2.Patients fulfilling the diagnostic criteria.
排除标准
- •1.Patients suffering from chronic Tonsillitis.
- •2.Complications like peritonsillar abscess and other systemic disorders.
结局指标
主要结局
1.Assessment will be made on the basis of improvement in the clinical features.
时间窗: 21days
b)Fever
时间窗: 21days
c)Tonsillar erythema or swelling
时间窗: 21days
2.Patients will be assessed as per the subjective and objective parameters made for the study.
时间窗: 21days
Subjective
时间窗: 21days
b) sore throat/pain during swallowing.
时间窗: 21days
d)Presence of exudates or plugs in tonsils
时间窗: 21days
a)Difficulties in a daily life
时间窗: 21days
Objective
时间窗: 21days
a)Pharyngeal erythema or swelling
时间窗: 21days
次要结局
- Assessment will be made on the basis of improvement in the clinical features.(a)Pharyngeal erythema or swelling)