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临床试验/NCT01215721
NCT01215721已完成不适用

Vesicare™ (Solifenacin) in the Treatment of Urinary Incontinence After Radical Prostatectomy

University of California, Irvine1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2010年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Time to Continence

研究概览

简要总结

Prostate cancer is the most common non-cutaneous malignancy in men and is the 2nd leading cause of death from cancer in men. Radical prostatectomy is one of the treatment options available for organ-confined disease. Over 100,000 radical prostatectomies cases (total removal of the cancerous prostate by surgery) are performed in the United States yearly. Unfortunately nearly all of the men undergoing surgery report diminished Quality of Life (QOL) scores due in part due to a postoperative incontinence which may require the use of multiple urinary pads per day. Many of these men also report debilitating irritative voiding symptoms of urinary urgency and frequency, and have overall decreased urinary satisfaction scores. Abatement of these symptoms can take up to one year in men, and in 5-20% of patients symptoms may persist for longer periods.

Our recent published findings suggest that instability in the bladder muscle is likely an underlying etiology in postoperative urinary incontinence. This 'Detrusor Muscle' instability results in excess contractions of the urinary bladder ('urgency to urinate'), and can result in the feeling of needing to urinate more frequently. Consistent with this hypothesis of detrusor muscle instability, men with postoperative dribbling had more complaints with urgency, frequency and bother scores when queried with validated questionnaires. We suspect that a transient bladder muscle contraction may overcome the urinary sphincter valve resistance and result in the patient's dribbling of urine.

By treating the bladder muscle instability, we expect improved postoperative continence and improved quality of life in patients after undergoing surgery for total removal of a cancerous prostate. This pilot study will assess the statistical requirements for the number of subjects needed for a fully 'powered' randomized prospective study to fully evaluate whether medications such as solifenacin significantly improve patients' quality of urinary life and improve postoperative urinary incontinence after surgery.

*This study has been modified from the original protocol with the clinicaltrials.gov ID: NCT00581061.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

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

  • Patients that have been diagnosed with prostate cancer and will undergo treatment for the disease as part of standard clinical care
  • Patients that have multiple pad use a few days after standard of care catheter removal

排除标准

  • Contra-indication to Solifenacin
  • Narrow angle glaucoma
  • Hepatic impairment
  • Renal impairment
  • CYP3A4 inhibitors (e.g. Ketoconazole)
  • Gastric Retention (delayed or slow emptying of the stomach)
  • Lives in a different country

研究组 & 干预措施

Vesicare

Experimental

Vesicare 5mg daily for 90 days was prescribed for men presenting with post-Robotic Assisted Radical Prostatectomy (RARP) severe incontinence.

干预措施: Vesicare (Drug)

结局指标

主要结局

Time to Continence

时间窗: 12 months

Days to zero pad continence were assessed by patient self-reported Pad free continence declaration card.

次要结局

未报告次要终点

研究者

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

Thomas E. Ahlering

Urology Account Contact

University of California, Irvine

研究点 (1)

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