At a glance
ClinicalIndex Comparison RecordN/ACompleted· 5 enrolled
Drug / intervention
Peritron+device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Human Factor Study To Asses The Usability And Feasibility Of The Peritron+ During Intended Use
In Brief
A clinical study evaluating Peritron+ for Urology. Completed, enrolled 5 participants.
Detailed Summary
In a hospital setting, the self-measurement of intravesical pressure (SMIP) assessment will be conducted at full and empty bladder using the Peritron+ and a ruler-based manometry method. In the home setting a human factor/usability study will be conducted to measure the subject's ability to perform a successful SMIP assessment at full and empty bladder with the Peritron+. This study involves the use of the Peritron+, Air-Trap Tubing, a ruler and a clean intermittent catheter (CIC).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsUrology
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartFeb 2016
First PostedApr 2016
Primary CompletionJul 2016
TodayJul 2026
First PostedApr 21, 2016
Enrollment StartFeb 1, 2016
Primary CompletionJul 1, 2016
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 10.2 years ago
Interventions
Peritron+device
Peritron+ device to measure intravesical pressure