Loading clinical trials...
Loading clinical trials...
Clinical Study of the Amedica Corporation Valeo OL Interbody Fusion Devices for Posterior Lumbar Interbody Fusion
This study randomizes degenerative spondylolisthesis and/or degenerative disc patients into two groups: one to receive a new ceramic implant and a control group with a more traditional PEEK plastic implant. The procedure uses a single oblique cage in each group. The study will measure and compare pain and disability improvement with the two implanted devices over a period of two years. The fusion status will also be judged with plane x-rays and one CT scan.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Medical Center Haaglanden
The Hague, Netherlands
Diakonessenhuis
Utrecht, Netherlands
Start Date
February 1, 2012
Primary Completion Date
January 1, 2016
Completion Date
March 1, 2017
Last Updated
April 4, 2017
100
ACTUAL participants
Posterior lumbar interbody fusion with a PEEK cage
DEVICE
Posterior lumbar interbody fusion with a Valeo OL cage
DEVICE
Lead Sponsor
Amedica Corporation
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions