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Clinical Trial Summary

This First In Human study is aimed to evaluate the safety and initial efficacy of the Vibe delivery system in delivering Botox (TM) to the bladder wall in patients diagnosed with overactive bladder.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03874780
Study type Interventional
Source Vensica Medical Ltd.
Contact
Status Completed
Phase N/A
Start date January 29, 2019
Completion date March 31, 2019

See also
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