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NCT Number: NCT06905808

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

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).

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Bristol Urological Institute

Bristol, United Kingdom

Location status: Recruiting

Location contact

Andrew Gammie, DPhil CEng CSci

PRINCIPAL_INVESTIGATOR

Victoria Garner

CONTACT

[email protected]

+0117 414 8109

About this study

Subjects who are referred to undergo a Urodynamics will be recruited to participate. Initial resting pressures will be measured/recorded using the e-Sense® and water-filled catheter (dual-catheterized) in lying, sitting, and standing positions for each subject. The study will collect various urodynamic pressure values at regular intervals during bladder filling. The detrusor pressures before filling will then be compared with the pressures collected during bladder filling to determine normal pressure value ranges. Urethral pressures will also be measured using e-Sense® and water-filled catheters, and the values compared. The goal is to provide users of the e-Sense® catheter as to what values should be expected when good quality measurements are being made.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

eSense 7Fr Single Sensor Bladder Catheter

Device

Urinary and abdominal catheters inserted into the body to measure pressure for urodynamics.

Other names: eSense 7Fr Abdominal Catheters, eSense 7Fr Dual Sensor Urethral Catheters

Primary outcomes

  1. To determine the range of normal pressure values for different patient positions measured by the e-Sense® catheter

    Time frame: Periprocedural, during Urodynamic Procedure

    The primary endpoint will be measured by recording the subject in three different positions (sitting, lying and standing) to determine a range normal pressures value. The values will be recorded on each subject case report form.

Secondary outcomes

  1. To compare pressure values measured by the e-Sense® catheters to the pressures simultaneously measured via a separate water filled catheters.

    Time frame: Periprocedural, during Urodynamic Procedure

    To investigate the change of pressures readings when the subject changes positions, a comparison would be made in the change of pressure recorded by both e-Sense® and water filled catheters when the subject moves from supine to sitting and from sitting to standing.

Sponsors and collaborators

Lead sponsor

Laborie Medical Technologies Inc.

Industry

Registry information

Acronym: ESNS-01

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 1, 2025
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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