Clinical Trials Directory

Trials / Completed

CompletedNCT02746406

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
5 (actual)
Sponsor
Laborie Medical Technologies Inc. · Industry
Sex
All
Age
2 Years – 18 Years
Healthy volunteers
Accepted

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).

Conditions

Interventions

TypeNameDescription
DEVICEPeritron+Peritron+ device to measure intravesical pressure

Timeline

Start date
2016-02-01
Primary completion
2016-07-01
First posted
2016-04-21
Last updated
2017-01-11
Results posted
2017-01-11

Source: ClinicalTrials.gov record NCT02746406. Inclusion in this directory is not an endorsement.