Portable Pves Study

Laborie Medical Technologies

Status: Completed

Conditions: Lower Urinary Tract Symptoms

Treatments: Device: Peritron+

Study type: Interventional

Funder types: Industry

Identifiers

NCT02673944

PLUS-PVES-01

Details and patient eligibility

About

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.

Enrollment: 10 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients normally indicated for urodynamic evaluation

Exclusion criteria

• Patients who suffer from bladder infections
• Patients who suffer from strictures in the urethra

Trial design

10 participants in 1 patient group

Peritron+

Experimental group

Description:

Patients will undergo a routine urodynamic evaluation, the Peritron+ will be used in conjunction with a water-based urodynamic catheter

Treatment:

Device: Peritron+