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临床试验/CTRI/2023/10/058595
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

发起方
Dr Muhammed Munavvir

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