CTRI/2021/06/034489尚未招募2 期
A RANDOMIZED CLINICAL STUDY TO EVALUATE THE EFFECTIVENESS OF DHANWANTARA TAILA AS UTTARA BASTI AND ORAL ADMINISTRATION IN THE MANAGEMENT OF VATASHTHEELA WITH SPECIAL REFERENCE TO BENIGN PROSTATE HYPERPLASIA
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Subject diagnosed as Benign Prostatic Hyperplasia by clinical and investigative methods will
- •be selected.
- •Patients having IPSS Score 7- 20 should be included.
- •In USG findings, patients having Prostate gland weight more than 40 gm and Residual Urine
- •Volume above 30 ml should be included.13
- •In uroflometry Qmax 3- 20 ml/s should be included.
排除标准
- •Patients with IPSS (International Prostate Symptom Score) above 20 (severe)
- •Patients having other systemic pathology like Tuberculosis, Renal Failure, Uncontrolled
- •Diabetes Mellitus And Uncontrolled Hypertension Etc..
- •Patients having other urinarysystem pathology like severe Urinary tract
- •infections, Nephrolithiasis, Urethral Stricture, Prostatitis
- •Patients suffering from Prostatic malignancy
- •Patients having congenital deformity of urogenital tract
- •HIV and HBsAg positive patients
- •Patients having PSA value above normal (above 10 ng/ml )should be excluded.
研究者
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