Medtronic: Spinal Diseases trials
The registry lists 13 Spinal Diseases studies with Medtronic as lead sponsor. 0 are open to participants now and 1 have results posted.
Phase 3 1No phase 12(a study in two phases counts in both)
Studies
Open to participants first, then studies with results posted, then the rest; newest registration first within each.
- Fenestrated Screw StudyTerminatedNCT03797144Not applicableResults posted
- Prospective, Observational Registry of Renaissance-guided Spine SurgeriesTerminatedNCT02212899
- MIS ReFRESH: Robotic vs. Freehand Minimally Invasive Spinal SurgeriesStatus unknownNCT02057744
- Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseTerminatedNCT01494493Not applicable
- Pilot Study of rhBMP/BCP With or Without the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01494441Not applicable
- A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseCompletedNCT01494428Not applicable
- INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot StudyCompletedNCT01491542Not applicable
- A Pivotal Study of rhBMP-2/ACS/INTER FIX™ Device for Posterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseTerminatedNCT01491464Not applicable
- A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491451Not applicable
- A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491425Not applicable
- Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseCompletedNCT01491386Not applicable
- A-MAV™ Anterior Motion Segment ReplacementCompletedNCT00635934Not applicable
- MAVERICK™ Total Disc Replacement- Pivotal StudyCompletedNCT00635843Phase 3