Medtronic Spinal and Biologics

26 total trials 1 currently recruiting 13 completed

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

RECRUITING NA

The Ailliance Post-Market Clinical Study

NCT05856370

ACTIVE NOT RECRUITING NA

Transforaminal Lumbar Interbody Fusion (TLIF)

NCT04073563

ACTIVE NOT RECRUITING NA

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

TERMINATED NA

Study of the Braive Growth Modulation System for Progressive Pediatric Scoliosis

NCT04929678

COMPLETED

Diffusion MRI-1 Imaging Database

NCT03775694

TERMINATED NA

An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical Spine

NCT03062657

COMPLETED

Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFUSE® in the Posterolateral Lumbar Spine

NCT02684045

TERMINATED

OLIF25™ /OLIF51™ Study

NCT02657421

COMPLETED Phase 2

A Study of MDT-10013 in the Treatment of Acute Postoperative Pain Following Bunionectomy

NCT02077140

COMPLETED Phase 2

A Study of the Pharmacokinetics, Safety, and Preliminary Efficacy of MDT-15 in Subjects With Lumbosacral Radiculopathy

NCT01917825

COMPLETED NA

Evaluation of Outcomes for Quality of Life and Activities of Daily Living for BKP in the Treatment of VCFs

NCT01871519

TERMINATED Phase 3

INFUSE®Bone Graft in Transforaminal Lumbar Interbody Fusion for Degenerative Disease of Lumbosacral Spine

NCT01415908

TERMINATED Phase 3

Tibial Delayed Healing Pivotal Clinical Trial

NCT01016067

TERMINATED

Localized Alveolar Ridge Augmentation With Dental Implant

NCT00991965

TERMINATED

Localized Alveolar Ridge Augmentation With Space Maintenance Devices

NCT00991432

TERMINATED

Sinus Augmentation With Dental Implant

NCT00991393

TERMINATED Phase 3

DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolateral Fusion

NCT00627497

COMPLETED NA

INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clinical Trial

NCT00485173

TERMINATED NA

Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Versus Conservative Care

NCT00456378

COMPLETED NA

Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels

NCT00637156

COMPLETED NA

A-MAV™ Anterior Motion Segment Replacement

NCT00635934

COMPLETED Phase 3

Study of Safety & Effectiveness of PRESTIGE® LP Cervical Disc vs. Anterior Cervical Fusion in Cervical DDD

NCT00667459

COMPLETED NA

Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of DDD Versus ACDF

NCT00437190

COMPLETED Phase 3

MAVERICK™ Total Disc Replacement- Pivotal Study

NCT00635843

COMPLETED NA

PRESTIGE® Cervical Disc Study

NCT00642876

COMPLETED Phase 3

rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study

NCT00707265

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.