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Clinical trial

A 2 and 5 Year Comparative Evaluation of Clinical Outcomes in the Treatment of Moderate Lumbar Spinal Stenosis With the Superion® Indirect Decompression System (IDS) vs. Direct Decompression Surgery for FDA Actual Conditions of Use Study

NCT03048955 is registered in ClinicalTrials.gov with VertiFlex, Incorporated as lead sponsor.

NCT NCT03048955
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Registry record

As filed in ClinicalTrials.gov.

Title
A 2 and 5 Year Comparative Evaluation of Clinical Outcomes in the Treatment of Moderate Lumbar Spinal Stenosis With the Superion® Indirect Decompression System (IDS) vs. Direct Decompression Surgery for FDA Actual Conditions of Use Study
Lead sponsor
VertiFlex, Incorporated
Phase
Not applicable
Overall status
Withdrawn
Start date
February 8, 2017
Completion date
July 31, 2025
Enrollment
0 (actual)
Sites
5

Conditions

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

spinal stenosis, lumbar region with neurogenic claudication