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Clinical Trial Summary

Instillation treatment with onabotulinumtoxin A (BOTOX®) in the urinary bladder


Clinical Trial Description

Pilot study to evaluate the effect of instillation treatment with onabotulinumtoxin A (BOTOX®) in the urinary bladder using Electromotive Drug Application (EMDA) in women with overactive bladder.

15 women with therapy-resistant OAB will be included. All patients must be qualified for conventional cystoscopic Botox injection. The study is not randomized or blinded. Follow-up time is six months with voiding charts and three questionnaires (Urinary Distress Inventory-6 (UDI-6), Incontinence Impact Questionnaire-7 (IIQ-7), International Consultation on Incontinence Questionnaire Urinary Incontinence Short Form (ICIQ-UI SF) as well as a satisfaction with treatment Visual analog scale (VAS). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02735499
Study type Interventional
Source The Hospital of Vestfold
Contact
Status Completed
Phase Phase 2
Start date March 2016
Completion date October 2016

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