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Clinical Trial Summary

A comparative study will be conducted and the patient will undergo a conventional urodynamic study. In order to successfully determine if the Peritron+ is capturing vesical pressure measurements consistent with conventional urodynamics the two sources of Pves will be collected concurrently.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


NCT number NCT02673944
Study type Interventional
Source Laborie Medical Technologies Inc.
Contact
Status Enrolling by invitation
Phase N/A
Start date January 2016
Completion date February 2016

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