RPCEC00000373尚未招募3 期
Comparative study of medium-term effects of Palmex (D-004), Saw palmetto,Finasteride and Tamsulosin in patients with Benign prostatic hyperplasia - D4SFTHPB
ational Centre for Scientific Research0 个研究点目标入组 200 人开始时间: 2021年5月27日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled trial. Masking: Open. Control group: Active. Assignment: Parallel. Purpose: Treatment
入排标准
- 年龄范围
- 40 years 至 80 years（—）
- 性别
- Male
入选标准
- •Those patients who meet the recruitment criteria (men = 40 years of age who have signed the informed consent and with mild or moderate lower urinary tract symptoms (LUTS). IPSS = 1, <19-) and with prostate enlargement verified by digital rectal examination.
排除标准
- •Patients with
- •Prostate cancer.
- •Previous history of urological surgery (prostate, bladder or urethral).
- •Urinary retention.
- •Prostate antigen (PSA) values> 4 ng / mL.
- •Presence of the middle lobe when performing transrectal ultrasound
- •History of liver failure.
- •History of chronic kidney failure.
- •Blood pressure> 180/110 mmHg.
- •Other active diagnosed neoplasms.
- •Alcoholism.
- •Psychiatric problems that limit the IPSS response.
- •Treatment with ADR-a1 antagonists, 5 a-reductase inhibitors, androgens, antiandrogens, cholinergics, anticholinergics, steroids and /or phytotherapeutic treatments in the 6 months prior to the study.
- •Usual clinical history of allergy to medications or any other special condition that, in the opinion of the doctor, puts your health and life at risk during the study
研究者
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