跳至主要内容
临床试验/CTRI/2024/07/071342
CTRI/2024/07/071342尚未招募不适用

A clinical study to evaluate the efficacy of rasa sindura orally and uttarvasthi with vasthyamayantak ghritam in the management of vatashtila mutraghata with special reference to benign prostatic hyperplasia

Dr BRKR GOVT AYURVEDIC MEDICAL COLLEGE AND HOSPITAL1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年8月19日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
30
试验地点
1
主要终点
Average change from base line of following parameters 1.PVR volume

研究概览

简要总结

This is a randomised clinical trial on efficacy of rasa sindura orally and uttravasthi with vasthyamayantak ghritam in the management of vatashtila (benign prostatic hyperplasia). Patients of age group 40-65 yrs who are diagnosed with vatashtila are taken for study.

The duration of treatment is 45 days.

Assessment will be done on every 15 days.

Follow-up after 45 days of completion of treatment.

研究设计

研究类型
Interventional

入排标准

年龄范围
40.00 Year(s) 至 65.00 Year(s)(—)
性别
Male

入选标准

  • Subjects who are presented with symptoms of vatashtila and confirmed by digital rectal examination and ultrasound scan.
  • Patients with PSA value less than 10.

排除标准

  • Patients with other cause of urinary tract symptoms like Neurogenic bladder Carcinoma prostate Urethral stricture Subjects with uncontrolled DM subjects with chronic renal failure and cardiac problems.

结局指标

主要结局

Average change from base line of following parameters 1.PVR volume

时间窗: Patients are monitored at time points day0 day15, day30, day45 and day90

2. Urinary symptoms like frequency, hesitancy, dribbling

时间窗: Patients are monitored at time points day0 day15, day30, day45 and day90

次要结局

  • Change in prostate volume(At day0, day15, day30, day45, & day90)

研究者

发起方
Dr BRKR GOVT AYURVEDIC MEDICAL COLLEGE AND HOSPITAL
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Chenna Abhilash

DR BRKR GOVT AYURVEDIC COLLEGE AND HOSPITAL

研究点 (1)

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