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NCT02677753 · ClinicalTrials.gov registry record · NA
Percutaneous Nerve Evaluation With Fluoroscopy Versus Without
A NA study, sponsored by University of Louisville.
- Completed
- Registry status
- NA
- Development phase
- 75
- Enrollment target
NCT02677753: Completed NA study, sponsored by University of Louisville.
NCT02677753 is a NA study that has completed, run by University of Louisville. The registered enrollment target is 75 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02677753, a NA study, has completed, sponsored by University of Louisville.
- COMPLETED
- Registry status
- NA
- Development phase
- 75 participants
- Enrollment target
Study Summary
The investigators propose a randomized control trial comparing the rate of implantation of the InterStim device following Percutaneous Nerve Evaluation (PNE) performed with or without fluoroscopic guidance.
Primary Outcome
Percentage of PNEs that have permanent neuromodulation device implanted by 3 months
Interventions
- RADIATION Fluoroscopy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2016-04 |
| Est. Completion | 2019-04 |
| Phase | NA |
What the finished NCT02677753 record still lists
NCT02677753 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 1 intervention - of which Fluoroscopy is the first listed.
NCT02677753 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02677753 about?
NCT02677753 is a clinical study titled "Percutaneous Nerve Evaluation With Fluoroscopy Versus Without". The investigators propose a randomized control trial comparing the rate of implantation of the InterStim device following Percutaneous Nerve Evaluation (PNE) performed with or without fluoroscopic guidance.
What is the current status of trial NCT02677753?
This trial is currently completed. It is a NA study. The enrollment target is 75 participants. The study started on 2016-04. Estimated completion is 2019-04.
What interventions are being tested in trial NCT02677753?
The interventions under investigation include: Fluoroscopy (RADIATION).
Who is sponsoring clinical trial NCT02677753?
This trial is sponsored by University of Louisville, which has 217 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02677753's enrollment target sits among peer trials
75 1069th of 2000 higher than 919 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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