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Vertos Mild - Post Market Patient Outcomes

2014-07-24 14:07:21 | BioPortfolio

Summary

This is a single-center study evaluating the outcomes of patients with painful lumbar spinal stenosis who were treated with the mild procedure (minimally invasive lumbar decompression. The patients will be followed for 6 months after the procedure.

Description

Approximately 50 patients at a single center will be enrolled and followed for a period of up to 26 weeks. Adult patients with symptomatic lumbar spinal stenosis who meet the enrollment criteria will be offered the mild procedure as an alternative to surgery or continued standard non-surgical medical management.

Study Design

Control: Uncontrolled, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Conditions

Lumbar Spinal Stenosis

Intervention

Minimally Invasive Lumbar Decompression

Location

The Center for Pain Relief, Inc
Charleston
West Virginia
United States
25301

Status

Recruiting

Source

The Center for Pain Relief, Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-07-24T14:07:21-0400

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