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临床试验/NCT03508921
NCT03508921终止4 期

Comparison of Methods for Prevention of Urinary Tract Infection Following Botox Injection: a Non-Inferiority Trial

Vanderbilt University Medical Center1 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2018年7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
终止
入组人数
22
试验地点
1
主要终点
Post Procedural- Urinary Tract Infection

研究概览

简要总结

Injection of OnabotulinumtoxinA (BTX-A) into the bladder is a widely used treatment option for patients with overactive bladder who have failed medical therapy. Urinary tract infection is the most common side effect of this procedure and therefore antibiotics are given around the time of injection in order to prevent these events. While antibiotics are commonly given at the time of injection, the duration of these antibiotic regimens are variable. The investigators propose a study to investigate different antibiotic protocols and their affect on the rate of urinary tract infection after injection.

详细描述

Intravesical injection of OnabotulinumtoxinA (BTX-A) is a widely practiced third line therapy for non-neurogenic overactive bladder (OAB). However, a paucity of data exists regarding urinary tract infections (UTI), the most common adverse event following injection. The investigators propose a randomized, controlled cross-over trial to investigate the utility of commonly practiced antibiotic protocols and simultaneously derive information regarding risk factors for post-procedural UTIs and their affect on treatment efficacy.

The investigators plan to initiate a prospective, randomized non-inferiority cross-over trial, in which a participant receives peri-procedural antibiotics exclusively at the time of one injection, and then at a subsequent injection, completes a three-day course of antibiotics post-operatively in addition to the peri-procedural dose. Enrollment is planned to achieve a total of 68 participants. Participants will be evaluated at 3 weeks and 3 months following injection to identify adverse events and treatment success. Inter-injection time will be measured and used a surrogate for efficacy over multiple injections.

These results, in addition to filling a void in current literature regarding the increasingly utilized treatment with BTX-A, have the potential to modify clinical practice regarding antibiotic use and decrease rates of adverse events. The means to stratify patients based on their specific risk of UTI may be used to facilitate antibiotic stewardship and improve patient outcomes.

研究设计

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

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Periprocedural Antibiotics Only

Experimental

Patients receive a one-time dose of antibiotics at the time of injection, prior to injection.

干预措施: Periprocedural Antibiotics (Drug)

Periprocedural Antibiotics Only

Experimental

Patients receive a one-time dose of antibiotics at the time of injection, prior to injection.

干预措施: Injection of OnabotulinumtoxinA (BTX-A) (Procedure)

Extended Antibiotics

Experimental

Patients receive a peri-procedural dose of antibiotics and an extended (3-day) course of antibiotics to be taken post-procedurally.

干预措施: Periprocedural Antibiotics (Drug)

Extended Antibiotics

Experimental

Patients receive a peri-procedural dose of antibiotics and an extended (3-day) course of antibiotics to be taken post-procedurally.

干预措施: Extended Antibiotics (Drug)

Extended Antibiotics

Experimental

Patients receive a peri-procedural dose of antibiotics and an extended (3-day) course of antibiotics to be taken post-procedurally.

干预措施: Injection of OnabotulinumtoxinA (BTX-A) (Procedure)

结局指标

主要结局

Post Procedural- Urinary Tract Infection

时间窗: 3 weeks post-injection

Number of participants with post procedural- urinary tract infection 3 weeks after injections, measured by a urine culture and defined as a urine culture with \>10\^5 bacterial colonies in the setting of urinary symptoms.

次要结局

  • Urinary Retention(3 weeks post-injection)
  • Recurrent Urinary Tract Infection(3 weeks post injection)

研究者

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

Melissa Kaufman

Associate Professor

Vanderbilt University Medical Center

研究点 (1)

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