CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 107 enrolled
Drug / intervention
The Spanner Temporary Prostatic Stentdevice
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.

Search/NCT02643849
NCT02643849N/ACompleted

Use of The Spanner® Temporary Prostatic Stent as an Alternative to a Urinary Catheter to Achieve Bladder Drainage in Men Unfit for Other Treatments

SRS Medical·interventional·Posted Dec 31, 2015·Updated Nov 19, 2020

In Brief

A clinical study evaluating The Spanner Temporary Prostatic Stent for Urinary Retention. Completed, enrolled 107 participants across 6 sites.

Detailed Summary

The Spanner is being evaluated for use to manage voiding dysfunction and lower urinary tract symptoms in subjects to achieve bladder drainage in men unfit for other treatments.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedDec 31, 2015
Enrollment StartAug 1, 2016
Primary CompletionJan 1, 2019
Study CompletionFeb 1, 2019
TodayJul 2, 2026
Enrollment to primary: 2.4 yearsPosted 10.5 years ago

Interventions

The Spanner Temporary Prostatic Stentdevice