e-Sense® Normal Values of Urodynamic Pressures Using e-Sense® Catheters

Recruiting now

Conditions studied: Lower Urinary Track Symptoms, Urodynamic Exam

In brief

In this post-market observational study, subjects referred to urodynamic testing will be approached to enroll in a clinical study to define the normal range of pressure values utilizing e-Sense® catheters. Urodynamic test results using the study devices will be provided back to the study sponsor for test interpretation and to publish. The urodynamic information collected using the study devices will be used in the UDS test interpretation for each subject enrolled, unless there is a reason to believe the test should be repeated (i.e. inconclusive results).

Key facts

Study ID

NCT06905808

Run by

Laborie Medical Technologies Inc.

People needed

40

Starts

2025-08-15

Expected to finish

2026-12-01

Last updated by the study team

2026-04-29

Who can join

Age: 20 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects medically indicated for Urodynamic procedure between ages 20-35 or > 50 years old (equally split male and female)
• Due to aging and giving birth significantly affecting the urethra:
• Female subjects 20-35 should be nulliparous.
• Female subjects > 50 years old should have given birth to at least one child vaginally. Further caesarian births would not mean exclusion from the study.
• Subjects with range of BMI values
• Subject provides written authorization and/or consent per institution or geographical requirements

You may not qualify if…

• Subjects with cognitive or psychiatric conditions that interfere with or precludes direct and accurate communication regarding the study, giving informed consent
• Any anal / rectal symptoms and/or surgery
• Pregnant women
• Subjects with active untreated bladder infections (not including patients with asymptomatic bacteruria)
• Subjects having greater than 300 mL post void residual on the clinic visit uroflowmetry test

Where it is running

• Bristol Urological Institute — Bristol, United Kingdom (enrolling)

Full record on ClinicalTrials.gov

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