At a glance
ClinicalIndex Comparison RecordN/ACompleted· 43 enrolled
Drug / intervention
PureWick Systemdevice
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 Prospective, Uncontrolled, Open-label Healthy Volunteer Study to Assess the Performance of the PureWick™ Male and PureWick™ Flex Female External Catheter Devices in Adolescents
In Brief
A clinical study evaluating PureWick System for Healthy Volunteers, Adolescent. Completed, enrolled 43 participants across 1 site.
Detailed Summary
A prospective, uncontrolled, open-label healthy volunteer study to assess the performance of the PureWick Male and PureWick Flex Female external catheter devices in adolescents
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHealthy Volunteers, Adolescent
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20252026
Enrollment StartAug 2024
Primary CompletionSep 2024
Study CompletionSep 2024
First PostedOct 2024
TodayJul 2026
First PostedOct 8, 2024
Enrollment StartAug 28, 2024
Primary CompletionSep 10, 2024
Study CompletionSep 25, 2024
TodayJul 2, 2026
Enrollment to primary: 12 daysPosted 1.7 years ago
Interventions
PureWick Systemdevice
The PureWick System consists of the PureWick Urine Collection System used with either the PureWick Male External Catheter or the PureWick Flex Female External Catheter, which are intended for non-invasive urine output management.