Post-Approval Study Protocol for the Simplify Cervical Artificial Disc

NACompletedINTERVENTIONAL
Enrollment

145

Participants

Timeline

Start Date

January 1, 2021

Primary Completion Date

April 23, 2023

Study Completion Date

April 23, 2023

Conditions
Cervical Degenerative Disc Disorder
Interventions
DEVICE

Simplify Disc

The Simplify Disc is a cervical artificial disc manufactured from polyether ether ketone (PEEK) endplates and a mobile, zirconia-toughened alumina ceramic core.

OTHER

ACDF

Historical ACDF control data

Trial Locations (15)

14094

Buffalo Spine Surgery, Lockport

20191

Virginia Spine Institute, Reston

28204

Carolina Neurosurgery and Spine Associates, Charlotte

34232

Kennedy-White orthopedic Center, Sarasota

42003

Orthopaedic Institute of Western Kentucky, Paducah

46032

Indiana Spine Group, Carmel

60201

NorthShore University Health System, Evanston

71101

Spine institute of Louisiana, Shreveport

75001

Texas Spine Consultants, Addison

75093

Texas Back Institute, Plano

80229

Spine Education and Research Foundation, Thornton

90403

The Spine Institute for Spine Restoration, Santa Monica

92121

USCD, San Diego

92868

Orthopaedic Education and Research Institute of Southern California, Orange

08234

Rothman Institute, Egg Harbor

Sponsors

Lead Sponsor

All Listed Sponsors
lead

NuVasive

INDUSTRY

NCT04630626 - Post-Approval Study Protocol for the Simplify Cervical Artificial Disc | Biotech Hunter | Biotech Hunter