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临床试验/ISRCTN46820623
ISRCTN46820623已完成未知

Accuracy of Bladder Ultrasound in the diagnosis of Detrusor Overactivity (DO): a study to evaluate if ultrasound can reduce the need for urodynamics

niversity of Birmingham (UK)0 个研究点目标入组 600 人开始时间: 2012年9月18日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
600

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

性别
Female

入选标准

  • 1. Frequency of 9 or more voids in 24 hours as reported in the 3 day bladder diary at least on one of the days
  • 2. Mild - severe urgency (cannot defer the urge to void) on at least one occasion in 3 day bladder diary
  • 3. Post void residual volume <100 mls on screening
  • 4. Written informed consent
  • 5. If patient has had previous stress incontinence surgery &/or Botox, it was >6 months ago

排除标准

  • 1. Pregnancy and up to 6 weeks postpartum
  • 2. Pure symptoms of stress incontinence or stress predominant mixed incontinence
  • 3. Evidence of cystitis (dipstick positive for leucocytes/nitrites)
  • 4. Voiding difficulties (post void residual >100 ml)
  • 5. Prolapse > grade II (any compartment)
  • 6. Urodynamics, assessment in the past 6 months
  • 7. Use of antimuscarinics for more than 6 months continuously.
  • 8. Current use of anti-muscarinics (e.g. Tolterodine, solifenacin, oxybutynin). If the woman is taking anti-muscarinics at the point of consent, she will be eligible if medication is ceased immediately
  • 9. There is a delay of at least 2 weeks until the index and reference tests are carried out.

研究者

发起方
niversity of Birmingham (UK)

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