Skip to main content
Clinical Trials/ISRCTN46820623
ISRCTN46820623
Completed
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 sites600 target enrollmentSeptember 18, 2012

Overview

Phase
未知
Intervention
Not specified
Conditions
Overactive bladder syndrome
Sponsor
niversity of Birmingham (UK)
Enrollment
600
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 18, 2012
End Date
TBD
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
niversity of Birmingham (UK)

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Not specified

Similar Trials