Rampart Duo Clinical (RaDical) Post-Market Study

CompletedOBSERVATIONAL
Enrollment

197

Participants

Timeline

Start Date

October 2, 2017

Primary Completion Date

April 21, 2022

Study Completion Date

October 3, 2022

Conditions
Lumbar Degenerative Disc Disease
Interventions
OTHER

"In this evaluation, no interventions are performed. It is a data collection effort only. The procedure for this study is the data collection effort."

There is no intervention performed in this evaluation. Data is being collected in an on-label standard of care lateral lumbar interbody fusion procedure.

Trial Locations (10)

17011

Orthopedic Institute of Pennsylvania, Camp Hill

20734

Georgetown University Hospital, Washington D.C.

33073

South Florida Spine & Orthopedics, Coconut Creek

42001

Orthopaedic Institute of Western Kentucky, Paducah

71101

Spine Institute of Louisiana, Shreveport

76182

Spine Works Institute, North Richland Hills

78705

Austin Spine Specialists, Austin

92354

Loma Linda University, Loma Linda

94538

Bell Neuroscience Institute/Washington Township Medical Foundation, Fremont

94558

Napa Valley Orthopaedic Medical Group, Napa

All Listed Sponsors
lead

Spineology, Inc

INDUSTRY

NCT03974711 - Rampart Duo Clinical (RaDical) Post-Market Study | Biotech Hunter | Biotech Hunter