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NCT02922868 · ClinicalTrials.gov registry record · NA
Assessment of Infection Control, Practice Efficiency, and Health Economics of Sheathed Versus Standard Cystoscopy
A NA study, sponsored by Wake Forest University Health Sciences.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT02922868: Completed NA study, sponsored by Wake Forest University Health Sciences.
NCT02922868 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02922868, a NA study, has completed, sponsored by Wake Forest University Health Sciences.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
The purpose of this research study is to compare the effectiveness and efficiency of using a sterile sheath (EndoSheath®) during cystoscopy versus a standard scope.
Primary Outcome
The primary endpoint will be the change in bacteriuria pre- and post-procedure between EndoSheath CST-5000 cystoscope and standard (non-sheathed) Olympus Visera Elite OTV-S190 cystoscope during the course of routine clinical use in a urology clinic. The pre-procedure measurement of bacteriuria will occur on the day of the procedure. The post-procedure measurement of bacteriuria will occur approximately two weeks (10-14 days) post-procedure. This will be assessed by urine culture exams.
Interventions
- DEVICE EndoSheath CST-5000 Scope
- DEVICE Olympus Visera Elite OTV-S190 Scope
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2016-03 |
| Est. Completion | 2016-12 |
| Phase | NA |
What the finished NCT02922868 record still lists
NCT02922868 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which EndoSheath CST-5000 Scope is the first listed.
NCT02922868 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02922868 about?
NCT02922868 is a clinical study titled "Assessment of Infection Control, Practice Efficiency, and Health Economics of Sheathed Versus Standard Cystoscopy". The purpose of this research study is to compare the effectiveness and efficiency of using a sterile sheath (EndoSheath®) during cystoscopy versus a standard scope.
What is the current status of trial NCT02922868?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2016-03. Estimated completion is 2016-12.
What interventions are being tested in trial NCT02922868?
The interventions under investigation include: EndoSheath CST-5000 Scope (DEVICE), Olympus Visera Elite OTV-S190 Scope (DEVICE).
Who is sponsoring clinical trial NCT02922868?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02922868's enrollment target sits among peer trials
60 1164th of 2000 higher than 745 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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