Medtronic Spinal and Biologics
Medtronic Spinal and Biologics sponsors 26 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 13 completed. 6 of these trials are in Phase 3-4 (later-stage) and 2 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Compression Fracture of Vertebral Body, with 1 trials.
Trial Pipeline
26 total, page 1 of 1
The Ailliance Post-Market Clinical Study
NCT05856370
Transforaminal Lumbar Interbody Fusion (TLIF)
NCT04073563
A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation for Posterolateral Fusion (PLF) Treatment of Multi-Level Degenerative Lumbosacral Spinal Conditions
NCT03118505
Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis
NCT04929678
Diffusion MRI-1 Imaging Database
NCT03775694
An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical Spine
NCT03062657
Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFUSE® in the Posterolateral Lumbar Spine
NCT02684045
OLIF25™ /OLIF51™ Study
NCT02657421
A Study of MDT-10013 in the Treatment of Acute Postoperative Pain Following Bunionectomy
NCT02077140
A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in Subjects With Lumbosacral Radiculopathy
NCT01917825
Evaluation of Outcomes for Quality of Life and Activities of Daily Living for BKP in the Treatment of VCFs
NCT01871519
INFUSE®Bone Graft in Transforaminal Lumbar Interbody Fusion for Degenerative Disease of Lumbosacral Spine
NCT01415908
Tibial Delayed Healing Pivotal Clinical Trial
NCT01016067
Localized Alveolar Ridge Augmentation With Dental Implant
NCT00991965
Localized Alveolar Ridge Augmentation With Space Maintenance Devices
NCT00991432
Sinus Augmentation With Dental Implant
NCT00991393
DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolateral Fusion
NCT00627497
INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clinical Trial
NCT00485173
Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Versus Conservative Care
NCT00456378
Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels
NCT00637156
A-MAV™ Anterior Motion Segment Replacement
NCT00635934
Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cervical Fusion in Cervical DDD
NCT00667459
Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of DDD Versus ACDF
NCT00437190
MAVERICK™ Total Disc Replacement- Pivotal Study
NCT00635843
PRESTIGE® Cervical Disc Study
NCT00642876
rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study
NCT00707265
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 2 | 2 |
| Phase 3 | 6 |
What the Pipeline for Medtronic Spinal and Biologics Shows
According to the ClinicalTrials.gov registry, Medtronic Spinal and Biologics is linked to 26 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 4% of the sponsor's indexed portfolio, and 13 are already marked complete, representing roughly 50% of the total.
The phase mix for Medtronic Spinal and Biologics reports 6 late-stage studies (Phase 3 and Phase 4 combined) and 2 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Medtronic Spinal and Biologics is Compression Fracture of Vertebral Body with 1 linked trial, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.