CTRI/2019/10/021513已完成4 期
Comparison of the efficacy of oxybutynin with that of mirabegron as an add-on therapy to tamsulosin in patients with persistent storage symptoms presumed to be due to benign prostatic hyperplasia : A randomized controlled trial
JAWAHARLAL INSTITUTE OF POSTGRADUATE MEDICAL EDUCATION RESEARCH0 个研究点目标入组 96 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 96
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
- •Male patients aged 50 years or older with LUTS presumed to be due BPH having urinary urgency at least once per week and a total OAB symptom score (OABSS) ââ?°Â¥ 3 points after ââ?°Â¥ 8 weeks treatment with tamsulosin 0.4mg od
排除标准
- •1.PVR > 100 ml
- •2.Q max < 5 ml/s
- •3.Prior diagnosis of neurogenic bladder
- •4.Performance of clean intermittent catheterization,
- •5.Severe bladder diverticulum or urethral stricture,
- •6.Planning to have a child,
- •7.Suspected prostate or bladder malignancy
- •8.Previous urethral surgery or prior diagnosis of urethral stricture disease.
- •9.Previous intra pelvic irradiation,
- •10.Suspected recurrent urinary infection,
- •11.Presence of renal or hepatic impairment,
- •12.Taking medicines contraindicated or requiring dose adjustments in combination with mirabegron or oxybutynin
- •13.Patients who have taken mirabegron or any anticholinergic medication in the previous 4 weeks.
- •14.Judged to be unsuitable for the trial by doctors
研究者
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