Rampart Duo Clinical (RaDical) Post-Market Study
Completed
- 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.
- First Posted Date
- 2019-06-05
- Last Posted Date
- 2023-12-01
- Lead Sponsor
- Spineology, Inc
- Target Recruit Count
- 197
- Registration Number
- NCT03974711
- Locations
- 🇺🇸
Orthopaedic Institute of Western Kentucky, Paducah, Kentucky, United States
🇺🇸Spine Institute of Louisiana, Shreveport, Louisiana, United States
🇺🇸Loma Linda University, Loma Linda, California, United States
Spineology Clinical Outcomes Trial: An IDE Investigation
Not Applicable
Completed
- Conditions
- Lumbar Degenerative Disc Disease
- Interventions
- Device: SIFS graft containment device
- First Posted Date
- 2015-01-27
- Last Posted Date
- 2021-10-20
- Lead Sponsor
- Spineology, Inc
- Target Recruit Count
- 102
- Registration Number
- NCT02347410
- Locations
- 🇺🇸
Georgetown University Hospital, Clinton, Maryland, United States
🇺🇸Spine Institute of Louisiana, Shreveport, Louisiana, United States
🇺🇸Florida Orthopaedic Associates, DeLand, Florida, United States
OptiMesh® for Lumbar Interbody Fusion Trial (OLIF)
Not Applicable
Completed
- Conditions
- Degeneration of Lumbar Intervertebral Disc
- Interventions
- Device: Structural Allograft SpacerDevice: OptiMesh 1500S
- First Posted Date
- 2008-10-02
- Last Posted Date
- 2021-09-16
- Lead Sponsor
- Spineology, Inc
- Target Recruit Count
- 156
- Registration Number
- NCT00764491
- Locations
- 🇺🇸
St. Charles Hospital, Port Jefferson, New York, United States
🇺🇸McLeod Health, Florence, South Carolina, United States
🇺🇸Fletcher-Allen Health Center, Burlington, Vermont, United States
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