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临床试验/CTRI/2023/08/056483
CTRI/2023/08/056483尚未招募2/3 期

Open Randomized Control Clinical Trial Of Efficacy Of Saindhawadi Churna In The Management Of Arsha With Special Reference To First And Second Degree Internal Hemorrhoids

Dr Nikhil Uttam Nigade1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年8月28日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
To Evaluate the efficacy of Saindhawadi Churna in management of Arsha

研究概览

简要总结

As we see the number of patients of Arsha are increasing day by day due to their sedentary lifestyle so this study will give relief from Arsha symptoms and other complications to patients . This study is randomized open controlled clinical trial to evaluate the efficacy of Saindhawadi Churna in management of arsha as a trial drug and Kankayan Vati as a control drug . Trial and control drugs administrates in the form of Churna and Vati respectively in diagnosed cases of arsha or first and second degree internal hemorrhoids for 7 days ie 2 gm by in a day . 10th day follow up day . 35 patients will be in each groups will be studied . Study will conduct in India . Outcome of study will be assess on reduction of symptoms of Arsha .

研究设计

研究类型
Interventional
分配方式
Other
盲法
Open Label

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 1 Patients presenting with the Lakshana of Arsha 2 Patients of both genders between the age group of 20 to 60 years 3 Patients of Internal Hemorrhoids of all position with First and Second degree of Internal Hemorrhoids.

排除标准

  • 1 Pregnancy and lactating women 2 Arshas associated with other anorectal colon conditions like Fissure Fistula in ano Polyps Ulcerative Colitis Sinus Malignancy Vascular Anomalies Abscess Bleeding Piles 3 Patients with Systemic Diseases like Hypertension Diabetes.

结局指标

主要结局

To Evaluate the efficacy of Saindhawadi Churna in management of Arsha

时间窗: 4 weeks

次要结局

  • To compare the efficacy of Saindhawadi Churna And Kankayan Vati in management of Arsha(4 Weeks)

研究者

发起方
Dr Nikhil Uttam Nigade
申办方类型
Other [self]

研究点 (1)

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