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临床试验/NCT07307261
NCT07307261已完成不适用

Evaluation of Mirabegron Versus Tamsulosin or Their Combination in Treatment of Lower Urinary Tract Symptoms Related to Double j Stent in Adults: A Prospective Randomized Study

Avraiem Talaat1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2024年10月10日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
300
试验地点
1
主要终点
Treatment of Ureteral Stent Pain

研究概览

简要总结

Stent related symptoms (SRSs) comprise of complaints such as irritative symptoms, sense of incomplete emptying, flank and suprapubic pain, and incontinence. Mechanical irritation of trigone, urinary reflux, and stent movement are plausible causes for SRSs.

Alpha-blockers are the primary medications for ureteral stent-related symptoms. These medications are suggested to patients by the American Urological Association (AUA)/Endourological Society guideline to reduce stent-related symptoms with moderate recommendation. Nevertheless, there are many side effects associated with alpha-blockers such as dizziness, headache, and orthostatic hypotension

详细描述

Ureteral stents have become an important part of urologic practice since first described the double-J stent . most often urolithiasis. Their use may be associated with significant bothersome symptoms and discomfort. Ureteral stent-related symptoms (SRSs) may occur in up to 88% of patients in mild or more severe degree.

Mirabegron is the first and only selective β3-adrenergic receptor agonist agent currently available and it is one of the treatment options for overactive bladder (OAB). Hence, many urologists have been introducing mirabegron therapy for OAB in recent years and because the SRS are similar to OAB symptoms, it may be another treatment option for reducing bladder irritability in patients indwelling DJ stent.

It is currently unclear whether mirabegron has a place in the treatment of SRSs. Our study aims to systematically evaluate the efficacy and safety of mirabegron in treating SRSs in comparison to Tamsulosin and their combination in adult patients

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • First time to use Ureteric stent .

排除标准

  • Urinary tract infection.
  • Previous ureteral surgery.
  • Congenital malformation of the ureter.
  • Distal ureteric stricture.
  • Hypersensitivity to the drugs.
  • Pregnancy or lactation.
  • Hepatic insufficiency
  • Non-compliant patients.
  • Age < 18 years old .

研究组 & 干预措施

Tamsulosin 0.4mg

Active Comparator

About 100 patients will receive Tamsulosin (0.4mg) once daily for 3 weeks for the treatment of lower urinary tract symptoms related to double j stent in adults

干预措施: Tamsulosin (Drug)

Mirabegron 50mg

Active Comparator

About 100 patients will receive Mirabegron (50mg) once daily for 3 weeks for the treatment of lower urinary tract symptoms related to double j stent in adults

干预措施: Tamsulosin (Drug)

combination of tamsulosin 0.4mg and Mirabegron 50mg

Active Comparator

About 100 patients will receive A combination of tamsulosin (0.4mg) and Mirabegron (50mg) once daily for 3 weeks for the treatment of lower urinary tract symptoms related to double j stent in adults

干预措施: Tamsulosin (Drug)

结局指标

主要结局

Treatment of Ureteral Stent Pain

时间窗: 4 Weeks

All patients will be evaluated before and after the treatment from the pain by the visual analog pain scale..

次要结局

未报告次要终点

研究者

发起方
Avraiem Talaat
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Avraiem Talaat

Resident at Urology Department

South Valley University

研究点 (1)

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