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Clinical trial

A Multicenter, Post Marketing Clinical Follow-up Study to Evaluate the Safety and Effectiveness of the Minimally Invasive Device APERIUS® in Degenerative Lumbar Spinal Stenosis With Symptomatic Neurogenic Intermittent Claudication

NCT00887744 is registered in ClinicalTrials.gov with Medtronic Spinal and Biologics as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Multicenter, Post Marketing Clinical Follow-up Study to Evaluate the Safety and Effectiveness of the Minimally Invasive Device APERIUS® in Degenerative Lumbar Spinal Stenosis With Symptomatic Neurogenic Intermittent Claudication
Lead sponsor
Medtronic Spinal and Biologics
Phase
Phase 4
Overall status
Completed
Start date
November 30, 2006
Completion date
March 31, 2010
Enrollment
162 (actual)
Sites
12

Conditions

As the registry lists them; a condition with its own page is linked.