A Single Arm Clinical Study To Evaluate The Efficacy Of Triphaladya Churna In The Management Of Vatashthila (Benign Prostatic Hyperplasia)

SHUBHAM SHARMA1 个研究点分布在 1 个国家目标入组 32 人开始时间: 2023年3月15日最近更新: 2022年12月23日

试验速览

阶段: 2/3 期
状态: 尚未招募
发起方
入组人数: 32
试验地点: 1
主要终点: To observe the efficacy of Triphaladya churna in the management of urine retention in Vatashthila (Benign Prostatic Hyperplasia)

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This is a Single Arm Clinical Study in which Triphaladya churna with Luke warm water will be carried out on 32 pre- diagnosed patients of Vatashthila ( Benign Prostatic Hyperplasia) for relieving urine retention due to BPH. Follow- ups will be on 7th and 15th day and total duration of the study will be 15 days. The age group taken for the study will be 45 years and upto 80 years.

研究设计

研究类型: Interventional
分配方式: Not Applicable
盲法: Not Applicable

入排标准

年龄范围: 45.00 Year(s) 至 80.00 Year(s)（—）
性别: Male

入选标准

•A) K/C/O Vatashthila.
•B) Patient having any of 3 sign & symptoms of disease like incomplete emptying, frequency, intermittency,urgency,weak stream, straining and nocturia.
•C) Male patient, irrespective of socio- economic status.

排除标准

•a) Bladder neck stenosis, bladder diverticulum, neurogenic bladder, neoplasm of bladder, urethral stricture.
•b) Patients with malignancy of prostate c) Patient with associated disease like T.B. , Leprosy, Venereal disease ,immuno- compromised.
•d) Patient with major complication like uremia , septicemia , shock, renal failure.

结局指标

主要结局

To observe the efficacy of Triphaladya churna in the management of urine retention in Vatashthila (Benign Prostatic Hyperplasia)

时间窗: Triphaladya churna oral administration 1 karsha with lukewarm water twice a day for 15 days. | Follow-up will be on 7th and 15th day. | Total duration of study will be 15 days.

次要结局

1) To provide safe and cost effective treatment(for relieving urine retention in benign prostatic hyperplasia.)

研究者

发起方

SHUBHAM SHARMA

申办方类型

Other [self]

研究点 (1)

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