A Randomized Controlled Clinical Trial To Assess The Efficacy Of Kushmanda Kalyanaka In Karshya.
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
- Patient will be checked for following symptoms:
研究概览
简要总结
This study is a randomized, single blind, parallel group, actively controlled clinical study with comparative standard drug - Ashwagandhadi Lehya and interventional drug - Kushmanda Kalyanaka Avaleha with the dosage12 gms (Total: 24gms per day) empty stomach before to the meals as BID. This study is conducting on patients of Karshya belongs to age of 16yrs to 60yrs who gives written and verbal consent for undergoing clinical study. Study will be conducting in Alvas Ayurveda Medical College and Hospital, Vidyagiri, Moodbidri. Interventional period of this study is 60 days. Assessment will be done on 0th Day, 46th Day, 61st 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
- 16.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients between the age group of 16 to 60 years.
- •Patient having at least one of the Nidana mentioned in Ayurvedic literature for Karshya will be included.
- •Patient willing to sign Written Consent Form.
排除标准
- •Patients with Karshyatha due to Tuberculosis, Malignancies and metabolic disorders.
- •Patients with any other systemic disorders which will interfere the study will be excluded.
结局指标
主要结局
Patient will be checked for following symptoms:
时间窗: 60 Days
2) Intolerence to Physical work
时间窗: 60 Days
3) Intolerence to Hunger and Thrist
时间窗: 60 Days
4) Prominent Joints And Bones
时间窗: 60 Days
1) Prominent Vascular Network
时间窗: 60 Days
次要结局
- The below Criteria will be Checked on 0Th day, 46th Day and 61st Day.(1) Weight)