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MiDAS I (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation Study

NCT00956631 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2013-04-04

Study results available
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Summary

This is a multi-center, prospective, clinical study to assess the clinical application and outcomes of MILD® Interlaminar Decompression in patients with symptomatic lumbar spinal stenosis.

Conditions

  • Lumbar Spinal Stenosis

Interventions

PROCEDURE

Interlaminar Decompression

The MILD® devices used in this study are specialized surgical instruments intended to be used to perform percutaneous lumbar decompression.

Sponsors & Collaborators

  • Vertos Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • David Caraway, MD · The Center for Pain Relief Tri-State, PLLC

  • Bohdan W Chopko, MD · MedCentral Health System

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-07-31
Primary Completion
2012-04-30
Completion
2012-04-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00956631 on ClinicalTrials.gov