Zimmer Biomet

115 total trials 12 currently recruiting 53 completed

Zimmer Biomet sponsors 115 registered US clinical trials on ClinicalTrials.gov, 12 of them currently recruiting, and 53 completed. 4 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 Rheumatoid Arthritis, with 13 trials.

Trial Pipeline

115 total, page 2 of 3

COMPLETED NA

Persona TM Tibia Clinical Outcomes Study

NCT03589300

COMPLETED NA

NexGen TM Tibia Clinical Outcomes Study

NCT03272373

COMPLETED

Evaluating Bactisure Wound Lavage in Orthopedic Wounds

NCT03192124

COMPLETED

A Cohort Study for Clinical Evaluation of OmniMax MMF System

NCT03075865

COMPLETED NA

BioWick SureLock Clinical Outcomes Study

NCT03199391

COMPLETED NA

Subchondroplasty® Knee RCT

NCT03112200

COMPLETED

A Longitudinal Outcomes Study of the Subchondroplasty® Procedure in the Foot/Ankle

NCT03087396

TERMINATED

Prospective Clinical Follow-up of the Echo Bi-Metric Microplasty Stem for Total Hip Arthroplasty

NCT04326010

COMPLETED NA

Saline-Controlled Study of nSTRIDE APS for Knee Osteoarthritis

NCT02905240

COMPLETED

Zimmer® MotionLoc® in Distal Tibia Fractures

NCT02717546

COMPLETED NA

BOLD MRI as a Surrogate of Improved Muscle Oxygenation Following Endovascular Therapy for the Treatment of CLI

NCT02601430

COMPLETED Phase 1

Safety of NStride Autologous Protein Solution in the Treatment of Knee Osteoarthritis (PROGRESS I)

NCT02262364

TERMINATED NA

Randomized Controlled Clinical Outcomes of the Vanguard XP Bicruciate Knee System

NCT02175576

COMPLETED NA

Cellentra Viable Cell Bone Matrix (VCBM) Anterior Cervical Discectomy and Fusion Outcomes Study (VCBM/MaxAn)

NCT02182843

COMPLETED NA

Zimmer POLAR - Total Knee Arthroplasty (TKA)

NCT01859130

COMPLETED NA

Comprehensive Shoulder System Nano IDE

NCT01936259

COMPLETED NA

Sidus Stem-Free Shoulder IDE Study

NCT01878253

COMPLETED

A Multicentre Observational Study to Evaluate Clinical Outcomes of the G7 Acetabular System

NCT02036931

COMPLETED NA

An Evaluation of Rigid Sternal Fixation in Supporting Bone Healing and Improving Postoperative Recovery

NCT01783483

COMPLETED

An MRI Investigation of Soft Tissues in Total Hip Arthroplasty

NCT01750606

TERMINATED

A Clinical Registry to Collect Patient Outcome Date for the BIOMET® Stimulator Systems

NCT01750840

TERMINATED

SCP® Observational Study of the Knee

NCT03110224

TERMINATED NA

Oxford Signature vs. Conventional Global Study

NCT01763684

COMPLETED

Evaluation of Subchondroplasty™ for Defects Associated With Bone Marrow Lesions

NCT01621893

TERMINATED NA

Dynesys Spinal System Post Market 522 Study

NCT01528072

COMPLETED NA

Comparison of the Aspen Device Versus Pedicle Screws for Supplemental Posterior Fixation in Lumbar Interbody Fusion

NCT01549366

TERMINATED

Aspen Spinous Process Fixation System for Use in PLF in Patients With Spondylolisthesis

NCT01560273

COMPLETED NA

Safety and Efficacy of the Oxford Cementless Partial Knee System

NCT01473134

COMPLETED

MaxAn Post Market Surveillance Validation

NCT01343693

COMPLETED

Continuum™ Metal Bearing System in Total Hip Arthroplasty

NCT03382652

TERMINATED

Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder Arthroplasty

NCT01480453

TERMINATED

Discovery Elbow Long-Term Survivorship

NCT01308463

COMPLETED

Post Market Surveillance to Evaluate the Effectiveness the Polaris Deformity Spinal System

NCT01220505

TERMINATED Phase 2

CopiOs Posterolateral Fusion Procedure

NCT01123850

TERMINATED NA

Safety and Efficacy Study of Autologous Concentrated Bone Marrow Aspirate (cBMA) for Critical Limb Ischemia (CLI)

NCT01049919

COMPLETED

Feasibility Study of Anti-inflammatory Cytokines in Whole Blood in Osteoarthritis Patients

NCT01050894

TERMINATED NA

Signature Personalised Patient Care System With the Vanguard Knee System Study

NCT01092312

COMPLETED NA

Study of Root Coverage With Acellular Dermal Matrix: Puros® Dermis Versus Alloderm®

NCT00881959

COMPLETED NA

CopiOs® Pericardium Membrane for Localized Alveolar Ridge Augmentation

NCT00889265

COMPLETED NA

Prospective Multicenter Post Approval Study of the LPS-Flex Mobile Bearing Knee

NCT00854295

TERMINATED Phase 4

Trilogy AB Acetabular Hip System Post Approval Study

NCT00715026

COMPLETED

Regenerex Tibial Tray Multi-Center Data Collection

NCT00859963

COMPLETED NA

Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain

NCT00819286

COMPLETED

Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion System

NCT00758719

TERMINATED NA

Clinical Outcomes of the Trinica(R) Anterior Lumbar Plate: Fixed Screws vs. Variable Screws

NCT00762723

COMPLETED

Pediatric Locking Nail for the Treatment of Femoral Fractures in Children

NCT00725894

TERMINATED NA

A Double-Blind Study on Adjunctive Use of PEMF in the Treatment of 5th Metatarsal Non-Union Fractures

NCT00586170

COMPLETED Phase 3

Durom(R) Hip Resurfacing System Multicenter Trial

NCT00746616

COMPLETED

CopiOs(TM) Bone Void Filler in the Post-Harvest Iliac Crest

NCT00768924

TERMINATED

Avascular Necrosis (AVN) Long-Term Follow-up

NCT00833430

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Phase Distribution

PhaseTrial count
Phase 1 1
Phase 2 1
Phase 3 3
Phase 4 1

What the Pipeline for Zimmer Biomet Shows

According to the ClinicalTrials.gov registry, Zimmer Biomet is linked to 115 US clinical trials across every stage of research activity. Of those, 12 studies are currently recruiting, about 10% of the sponsor's indexed portfolio, and 53 are already marked complete, representing roughly 46% of the total.

The phase mix for Zimmer Biomet reports 4 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 Zimmer Biomet is Rheumatoid Arthritis with 13 linked trials, 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.