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临床试验/NCT07377929
NCT07377929招募中不适用

Intradetrusor Onabotulinumtoxin A (Botox) at the Time of Transurethral Resection of the Prostate or Transurethral Waterjet Ablation of the Prostate for Mixed Lower Urinary Tract Symptoms

Benaroya Research Institute1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2026年1月19日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
20
试验地点
1
主要终点
To identify whether concurrent Botox and TURP or Aquablation are effective at reducing post-operative irritative voiding symptoms.

研究概览

简要总结

Patients with longstanding obstructive lower urinary tract symptoms (LUTS) due to benign prostatic hypertrophy (BPH) can also develop symptoms of overactive bladder syndrome (OAB). Transurethral resection of the prostate (TURP) and Transurethral Waterjet Ablation of the Prostate (Aquablation) are amongst the gold standard surgical treatments for BPH. However, in the immediate post-operative period, TURP and Aquablation can also include OAB-like symptoms, including urinary frequency and urgency. For men with baseline OAB symptoms, this initial worsening of symptoms can be distressing.

Botox is an FDA approved medication with on-label indications to treat overactive bladder.

The purpose of this study is to evaluate the outcomes of men who have Botox concurrent with their TURP or Aquablation.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Male >= 18 years of age and being scheduled to undergo TURP or Aquablation and Botox procedure.
  • Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.

排除标准

  • Non-English speaking
  • Presence of a condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
  • History of receiving Botox in the bladder, within the previous 12 months.

研究组 & 干预措施

Observational Group

This group will contain men (>=18 years) and will be scheduled to undergo TURP or Aquablation and Botox procedure.

干预措施: Survey using a questionnaire. (Other)

结局指标

主要结局

To identify whether concurrent Botox and TURP or Aquablation are effective at reducing post-operative irritative voiding symptoms.

时间窗: 4 months

This will be measured using Postoperative Urinary Retention (POUR): At 1 week post-operative visit for trial of void to assess for rates of postoperative urinary retention. At 4 and 12 week post-operative visits for post void residual assessment

次要结局

  • To identify whether concurrent Botox and TURP or Aquablation lead to longer hospitalizations.(4 months)
  • To identify whether concurrent Botox and TURP or Aquablation lead to higher rates of urinary retention.(4 months)

研究者

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

Will Fuller

Principal Investigator

Benaroya Research Institute

研究点 (1)

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