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
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
Dr Chenna Abhilash
DR BRKR GOVT AYURVEDIC COLLEGE AND HOSPITAL
