CTRI/2023/10/058595尚未招募4 期
A Prospective open label study to evaluate the safety, efficacy and tolerability of mirabegron with solifenacin combination compared to their monotherapies in overactive bladder patients. - NI
Dr Muhammed Munavvir0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •OAB symptoms since 3 weeks
- •1 week drug free period for OAB treatment (mirabegron remains 5-6 days to be completely eliminated from the body [18])
- •Newly diagnosed OAB patient
- •Patients of both gender
排除标准
- •Known case of Pregnant and lactating women
- •Neurogenic bladder
- •Patient with significant stress/ urge
- •UTI, prostatis, interstitial cystitis, bladder stone, malignant pelvic disease
- •Urinary retention
- •End Stage Renal Disease
- •Diabetic nephropathy
- •Uncontrolled Hypertension[14] (Systolic pressure =180mmHg and diastolic pressure =110mmHg)
研究者
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