Clinical trial
Neurogenic Intermittent Claudication Evaluation Study
NCT00905359 · Medtronic Spinal and Biologics, Industry · Completed
Key facts
| NCT number | NCT00905359 |
|---|---|
| Title | Neurogenic Intermittent Claudication Evaluation Study |
| Official title | A Multicenter Prospective Randomized Controlled Clinical Trial to Evaluate the Effectiveness and Safety of the Aperius™ PercLID™ System Versus Standalone Decompressive Surgery in Degenerative Lumbar Spinal Stenosis With Neurogenic Intermittent Claudication |
| Acronym | NICE |
| Lead sponsor | Medtronic Spinal and Biologics, Industry |
| Status | Completed |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Spinal Stenosis |
| Intervention type | Procedure |
| Interventions | Aperius™ PercLID™ System, Standalone Decompressive Surgery |
| Enrollment | 163 |
| Start date | Jan 1, 2010 |
| Primary completion | Sep 1, 2014 |
| Completion | Apr 1, 2015 |
| First posted | May 20, 2009 |
| Last update posted | Feb 10, 2017 |
| Countries | Australia, Belgium, France, Germany, Iceland, Italy, Poland, Singapore, Sweden, United Kingdom |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: