NCT03532945View on ClinicalTrials.gov

A Follow-up Study to Evaluate the Efficacy and Safety of Novomax in Posterior Lumbar Interbody Fusion

NACompletedINTERVENTIONAL

Enrollment

62

Participants

Timeline

Start Date

October 28, 2010

Primary Completion Date

September 13, 2013

Study Completion Date

April 7, 2016

Conditions

Degenerative Lumbar Spinal Stenosis

Interventions

DEVICE

Bioactive Glass-Ceramic Spacer

DEVICE

Titanium cage

Sponsors

Lead Sponsor

All Listed Sponsors

lead

BioAlpha Inc.

INDUSTRY