Medtronic: Intervertebral Disc Degeneration trials
The registry lists 33 Intervertebral Disc Degeneration studies with Medtronic as lead sponsor. 2 are open to participants now and 7 have results posted.
Phase 3 3No phase 30(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.
- MDT-0123 Japan StudyRecruitingNCT07414745Phase 3
- A Post Market Surveillance on INFUSE Bone GraftRecruitingNCT05299762
- An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical SpineTerminatedNCT03062657Not applicableResults posted
- 5-Year Global Study on MAST™ Minimally Invasive Fusion Procedures to Treat Degenerative Lumbar Spine (MASTERS-D2)CompletedNCT02617563Results posted
- Maverick Total Disc Replacement in a 'Real World' Patient PopulationCompletedNCT01338493Results posted
- Satellite™ PEEK Nucleus Replacement Retrospective AnalysisCompletedNCT01110967Results posted
- Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cervical Fusion in Cervical DDDCompletedNCT00667459Phase 3Results posted
- Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent LevelsCompletedNCT00637156Not applicableResults posted
- INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clinical TrialCompletedNCT00485173Not applicableResults posted
- Prospective Clinical Study to Evaluate the Efficacy of the Stand-alone Cervical Interbody Cage C-CURVE ( Titanium) Manufactured by MEDICREA®CompletedNCT04547959Not applicable
- Titan Spine Endoskeleton TT/TO StudyTerminatedNCT03910309
- Personalized Spine Study Group RegistryWithdrawnNCT03843476
- OLIF25™ /OLIF51™ StudyTerminatedNCT02657421
- Spinal Cord Stimulation (SCS) Therapy StudyWithdrawnNCT02371122Not applicable
- Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instability Requiring Surgical FusionCompletedNCT01495234Not applicable
- Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseTerminatedNCT01494493Not applicable
- Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01494454Not 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
- rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level)CompletedNCT01491568Not applicable
- INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot StudyCompletedNCT01491542Not applicable
- TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot StudyCompletedNCT01491516Not applicable
- INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical Plate System Pivotal TrialTerminatedNCT01491477Not 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
- INFUSE™ BONE GRAFT/CORNERSTONE-SR™ Allograft Ring/ATLANTIS™ Anterior Cervical Plate- Pilot StudyCompletedNCT01491399Not applicable
- Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseCompletedNCT01491386Not applicable
- Pilot Study of rhBMP-2/ACS/LT-CAGE® for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491373Not applicable
- rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal StudyCompletedNCT00707265Phase 3
- PRESTIGE® Cervical Disc StudyCompletedNCT00642876Not applicable
- Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Versus Conservative CareTerminatedNCT00456378Not applicable
- Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of DDD Versus ACDFCompletedNCT00437190Not applicable