MedTrace Logo

Clinical Outcome and Fusion Results Using the VerteLoc® Facet Fixation Device

NCT01892878 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2018-03-16

No results posted yet for this study

Summary

The purpose of this clinical study is to evaluate fusion of the facet joints in a prospective cohort of patients utilizing the VerteLoc facet fixation device in patients receiving lumbar laminectomy (L1-S1), without ancillary stabilization devices such as pedicle and transfacet screws.

Conditions

  • Spinal Stenosis

Interventions

PROCEDURE

VerteLoc

Single Arm

Sponsors & Collaborators

  • VG Innovations, LLC

    lead INDUSTRY

Principal Investigators

  • Lisa Guyot, MD · Ascension Health

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-31
Primary Completion
2015-07-31
Completion
2016-01-01

Countries

  • United States

Study Locations

More Related Trials

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 NCT01892878 on ClinicalTrials.gov