Post Approval Study Protocol for the Two Level Simplify® Cervical Artificial Disc

CompletedOBSERVATIONAL
Enrollment

291

Participants

Timeline

Start Date

August 1, 2021

Primary Completion Date

January 24, 2024

Study Completion Date

January 24, 2024

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.

Trial Locations (18)

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

46845

Parkview Research Center, Fort Wayne

48073

William Beaumont Hospital Research Institute, Royal Oak

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

84088

The Disc Replacement Center, West Jordan

90403

The Spine Institute for Spine Restoration, Santa Monica

92868

Orthopaedic Education and Research Institute of Southern California, Orange

97477

Oregon Neurosurgery, Springfield

06518

Connecticut Orthopaedic Specialists, Hamden

Sponsors

Lead Sponsor

All Listed Sponsors
lead

NuVasive

INDUSTRY

NCT04980378 - Post Approval Study Protocol for the Two Level Simplify® Cervical Artificial Disc | Biotech Hunter | Biotech Hunter