Status:
WITHDRAWN
A Follow-net Investigation of a Randomised Study of Cystoscopy and Urethral Dilatation Versus Cystoscopy Alone in Women With Overactive Bladder Syndrome and Impaired Voiding
Lead Sponsor:
Medway NHS Foundation Trust
Conditions:
Overactive Bladder
Voiding Dysfunction
Eligibility:
FEMALE
18+ years
Brief Summary
Urinary incontinences is a highly prevalent and distressing condition which has a significant impact on health related quality of life in millions of women worldwide. Of all women with incontinence, 9...
Detailed Description
Urinary incontinences is a highly prevalent and distressing condition which has a significant impact on health related quality of life in millions of women worldwide. Of all women with incontinence, 9...
Eligibility Criteria
Inclusion
- Significant Overactive Bladder Symptoms
- Based on scoring 1 or 2 on the Urgency Perception Scale
- On the symptoms domain of the KHQ
- More than 8 voids per day on frequency volume chart +/- 2 or more episodes of nocturia
- Pressure flow studies demonstrate a maximum flow rate of less than 15ml on a minimum voided volume of 200ml with a high or normal detrusor pressure at maximum flow or post-void residual of 200ml or over
- Patients must be able to give informed consent for the study.
Exclusion
- Presence of concurrent urodynamic stress incontinence.
- Patients with bladder pathology or haematuria of unknown origin.
- Patients with neurological disorders (as these may affect voiding).
- Symptomatic pelvic organ prolapse requiring intervention
- Patients with bladder pathology (including urinary tract infection) or haematuria of unknown origin
Key Trial Info
Start Date :
August 1 2016
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
December 1 2016
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT02297178
Start Date
August 1 2016
End Date
December 1 2016
Last Update
October 17 2016
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