Bristol Urological Institute
Bristol, United Kingdom
Location status: Recruiting
Location contact
Andrew Gammie, DPhil CEng CSci
PRINCIPAL_INVESTIGATOR
Victoria Garner
CONTACT
NCT Number: NCT06905808
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).
Interested in participating?
Request Info20 year and older
All sexes
Observational
Bristol, United Kingdom
Location status: Recruiting
Andrew Gammie, DPhil CEng CSci
PRINCIPAL_INVESTIGATOR
Victoria Garner
CONTACT
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
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.
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.
Laborie Medical Technologies Inc.
Industry
Acronym: ESNS-01
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.
Published trials that share one or more normalized conditions with this study.
NCT06834152
Adenocarcinoma, Carcinoma
Heidelberg, Baden-Wurttemberg, Germany
View Trial DetailsNCT07614321
Autoimmune Diseases, Autoimmune Diseases of the Nervous System
Morristown, New Jersey, United States
View Trial DetailsNCT07563764
Bladder, Bladder, Overactive
Kaohsiung, Taiwan
View Trial DetailsNCT07562386
Benign Prostate Obstruction (BPO), Lower Urinary Track Symptoms
Hamar, Norway
View Trial Details