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NCT02643849 · ClinicalTrials.gov registry record · NA
Use of The Spanner Temporary Prostatic Stent as an Alternative to a Urinary Catheter to Achieve Bladder Drainage in Men
A NA study of Urinary Retention, sponsored by SRS Medical.
- Completed
- Registry status
- NA
- Development phase
- 107
- Enrollment target
- 6
- Study locations
NCT02643849 is a NA study of Urinary Retention that has completed, run by SRS Medical. The registered enrollment target is 107 participants, below the 130-participant average among 11 other Urinary Retention trials with a reported enrollment target (18% lower). The trial reports 6 study locations across 3 states.
The verdict
NCT02643849, a NA study of Urinary Retention, has completed, sponsored by SRS Medical.
- COMPLETED
- Registry status
- NA
- Development phase
- 107 participants
- Enrollment target
- 6
- Study locations
Study 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.
Conditions Studied
Interventions
- DEVICE The Spanner Temporary Prostatic Stent
Study Locations (6)
Florida
- Atlantic Urology - Daytona Beach
- Advanced Urology Specialists - Oxford
- Urology Specialists of West Florida - Palm Harbor
- Pinellas Urology Inc - South Pasadena
Massachusetts
- Greater Boston Urology - Hingham
New York
- Brooklyn Urology Research Group - Brooklyn
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 107 participants |
| Start Date | 2016-08 |
| Est. Completion | 2019-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02643849
The ClinicalTrials.gov registry entry for NCT02643849 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 107 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 130-participant average among 11 other Urinary Retention trials with a reported enrollment target (18% lower). The listed sponsor is SRS Medical, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Urinary Retention appearing as the primary indexed condition, and to 1 intervention - of which The Spanner Temporary Prostatic Stent is the first listed.
NCT02643849 reports 6 study locations spanning 3 distinct geographic areas - top geographies include Florida, Massachusetts, New York.
Frequently Asked Questions
What is clinical trial NCT02643849 about?
NCT02643849 is a clinical study titled "Use of The Spanner Temporary Prostatic Stent as an Alternative to a Urinary Catheter to Achieve Bladder Drainage in Men". 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.
What is the current status of trial NCT02643849?
This trial is currently completed. It is a NA study. The enrollment target is 107 participants. The study started on 2016-08. Estimated completion is 2019-02.
What conditions does trial NCT02643849 study?
This clinical trial studies the following conditions: Urinary Retention.
What interventions are being tested in trial NCT02643849?
The interventions under investigation include: The Spanner Temporary Prostatic Stent (DEVICE).
Who is sponsoring clinical trial NCT02643849?
This trial is sponsored by SRS Medical, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02643849 being conducted?
This trial has 6 study locations across Florida, Massachusetts, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
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