N/A
N=10
Portable Pves Study
Lower Urinary Tract Symptoms
Bottom Line
View on ClinicalTrials.gov: NCT02673944 ↗Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Jun 2016
Primary outcome: Primary: Accurate Vesical PRessure — 18.56; 17.45 cm H2O
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Peritron+ (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Laborie Medical Technologies Inc.
- Primary completion
- Mar 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Accurate Vesical PRessure |
18.56; 17.45 | — |
Summary
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.
Eligibility Criteria
Inclusion Criteria
- Patients normally indicated for urodynamic evaluation
Exclusion Criteria
- Patients who suffer from bladder infections
- Patients who suffer from strictures in the urethra
Data sourced from ClinicalTrials.gov (NCT02673944). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.