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A Human Factor Study To Asses The Usability And Feasibility Of The Peritron+ During Intended Use

Urology Clinical Trial

Clinical Trial Summary

In a hospital setting, the self-measurement of intravesical pressure (SMIP) assessment will be conducted at full and empty bladder using the Peritron+ and a ruler-based manometry method. In the home setting a human factor/usability study will be conducted to measure the subject's ability to perform a successful SMIP assessment at full and empty bladder with the Peritron+. This study involves the use of the Peritron+, Air-Trap Tubing, a ruler and a clean intermittent catheter (CIC).

Clinical Trial Description

n/a

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02746406
Study type Interventional
Source Laborie Medical Technologies Inc.
Contact
Status Enrolling by invitation
Phase N/A
Start date February 2016
View Details
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