A randomized controlled clinical study to evaluate theEfficacy of peruka churna pratisarana in management ofMukhapaka in children
试验速览
- 阶段
- 2/3 期
- 状态
- 已完成
- 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
研究概览
简要总结
This study is randomized, parallel group, actively controlled clinical study with comparative standard
study- Khadira churna and interventional drug- Peruka churna with the dosage of 6gm in 3 divided doses. The study is conducting on patients of Mukhapaka belongs to age of
10years to 16years who gives written and verbal consent 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 7 days assessment will be done on before treatment, 3rd day,
7th day and followup on 14th 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
- 10.00 Year(s) 至 16.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients of either gender aged between 10 to 16 years.
- •Patient fulfilling the diagnostic criteria of mukhapaka will be selected.
排除标准
- •Children with congenital anomalies.
- •Children with other systemic illness.
- •Traumatic ulcers and infective stomatitis are excluded.
结局指标
主要结局
1. Assessment will be made on the basis of improvement in the clinical
时间窗: 14days
features.
时间窗: 14days
2. Patients will be assessed as per the subjective and objective parameters
时间窗: 14days
made for the study.
时间窗: 14days
Subjective
时间窗: 14days
a. Vyatha
时间窗: 14days
c. Lala srava atyartha
时间窗: 14days
b. Daha
时间窗: 14days
Objective
时间窗: 14days
a. Vrana sankhya
时间窗: 14days
b. Vrana pramana
时间窗: 14days
次要结局
- oral hygiene(14days)