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临床试验/NCT05968885
NCT05968885招募中4 期

Evaluation of the Efficacy and Urodynamic Outcomes Between Intradetrusor onabotulinumtoxinA Injection and Combination Pharmacotherapy in Patients With Detrusor Overactivity

Mackay Memorial Hospital1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2021年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
入组人数
300
试验地点
1
主要终点
Short form of Incontinence Impact Questionnaire (IIQ-7)

研究概览

简要总结

To investigates the effects of botulinum toxin type A bladder injection compared to combined pharmacotherapy with Mirabegron and Solifenacin.

详细描述

Patients with detrusor overactivity who were refractory to monotherapy with either anti-muscarinics or β3-adrenoceptor agonists were enrolled for prospective study. Patient were divided in two groups, intradetrusor onabotulinumtoxinA injection and combined pharmacotherapy with Mirabegron and Solifenacin. Incontinence-related symptoms distress and impact on quality of life were evaluated by short form of Urinary Distress Inventory, (UDI-6), Incontinence Impact Questionnaire (IIQ-7) and Overactive Bladder Symptom Score (OABSS). Objective outcomes include changes from baseline in daily urgency episodes, urinary incontinence episodes, maximum cystometric capacity, maximum detrusor pressure (Pdetmax) at first involuntary detrusor contraction and volume at first involuntary detrusor contraction were measured.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 90 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients with detrusor overactivity which defined as a urodynamic observation characterized by involuntary detrusor contractions during the filling phase. Those who were refractory to monotherapy with either anti-muscarinics or β3-adrenoceptor agonists were enrolled for prospective study

排除标准

  • Postvoid urine retention before treatment

研究组 & 干预措施

Intradetrusor onabotulinumtoxinA injection

Active Comparator

The toxin produced by Clostridium botulinum binds to the nerves endings and inhibits the muscular contractions, help to treat overactivity of the bladder muscles.

干预措施: Intradetrusor Botox® (onabotulinumtoxinA) injection (Procedure)

Combination pharmacotherapy

Experimental

Combine Mirabegron and Solifenacin.

干预措施: Combine Mirabegron and Solifenacin. (Drug)

结局指标

主要结局

Short form of Incontinence Impact Questionnaire (IIQ-7)

时间窗: Assess before treatment and 1 month, 3 months, 6 months and 1 year after treatment

The IIQ-7 assess the impact of urinary incontinence on QoL. 7 items assess influence of urinary incontinence on physical activity, travel, social/relationships \& emotional health. Each item is scored between 0 (activities not affected at all) to 3 (activities greatly affected). The total score ranges from 0 to 21, with a higher score indicating more severe of incontinence.

Short form of Urinary Distress Inventory (UDI-6)

时间窗: Assess before treatment and 1 month, 3 months, 6 months and 1 year after treatment

UDI-6 is a valid questionnaire, used particularly to investigate symptoms associated with lower urinary tract dysfunction and inquire on irritative, stress, and obstructive or discomfort complaints. UDI-6 consists of six items: frequent urination; leakage related to feeling of urgency; leakage related to activity, coughing, or sneezing; small amounts of leakage (drops); difficulty emptying the bladder; and pain or discomfort in the lower abdominal or genital area. The total score ranges from 0 to 18 , with a higher score indicating more severe of incontinence.

Overactive Bladder Symptom Score (OABSS)

时间窗: Assess before treatment and 1 month, 3 months, 6 months and 1 year after treatment

The total OABSS is the sum of four symptom scores: daytime frequency (score 0-2), nighttime frequency (score 0-3), urgency (score 0-5), and urgency incontinence (score 0-5). The total score ranges from 0 to 15, with a higher score indicating more severe of OAB symptoms.

次要结局

  • Maximum cystometric capacity(Assess during 3 months - 1year after treatment)
  • Maximum detrusor pressure at first involuntary detrusor contraction(Assess during 3 months - 1year after treatment)
  • Volume at first involuntary detrusor contraction(Assess during 3 months - 1year after treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hui-Hsuan Lau, MD

Head of urogynecology, Associate Professor

Mackay Memorial Hospital

研究点 (1)

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