Stryker Trauma and Extremities
Stryker Trauma and Extremities sponsors 30 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 11 completed. 1 of these trials are in Phase 3-4 (later-stage) and 0 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Femoral Fracture, with 3 trials.
Trial Pipeline
30 total, page 1 of 1
A Prospective, Post-Market, Clinical Follow-up Study of the Incompass™ Total Ankle System
NCT07118501
Perform Humeral System Study
NCT05067543
Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical Study
NCT05868148
Perform® Humeral System - Fracture Study (PFX)
NCT05773352
Post Market Clinical Evaluation of Gamma 4
NCT05523635
Pyrocarbon Clinical Follow-up Study
NCT05049993
INFINITY™ With ADAPTIS™ Technology Study
NCT04594993
A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the Femoral Nail PF
NCT04015154
A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the Femoral Nail GT
NCT04015128
Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients Suffering From Lateral Ankle Instability
NCT06829667
Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction of the Anterior Talofibular Ligament (ATFL) to Treat Lateral Ankle Instability
NCT06638138
Lower Extremity Fixation In Neuropathic Patients Study
NCT04607044
Wright Foot & Ankle Post-Market Observational Study
NCT04118894
A Post-Market Clinical Evaluation of the ReUnion Reversible Fracture (RFX) System
NCT04089371
A Post-Market Clinical Evaluation of the Treatment of Tibia Fractures With the T2 Alpha Tibia Nailing System
NCT04015167
Collecting Orthopedic Safety and Performance Data Using Surgeons Clinical Outcomes Registry (SCOR)
NCT04032444
A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty (RSA) System
NCT03880955
A Post-Market Clinical Evaluation of the ReUnion TSA System
NCT03858517
INFINITY™Total Ankle Replacement Follow-up
NCT03277989
Aequalis Pyrocarbon IDE; Replacing the Humeral Head in Hemi-Arthroplasty
NCT02525783
Tornier Shoulder Outcomes Study to Examine Safety and Functional Outcomes in Shoulder Arthroplasty and Fracture Patients
NCT02047955
BioFiber Scaffold Post-Market Observational Study
NCT01849458
Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation
NCT01380444
Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder Arthroplasty
NCT01390038
INBONE™ Total Ankle Prosthesis With Long Talar Stem
NCT01641848
INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation
NCT01366989
Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot Ulcers
NCT01353495
Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR Ankle Among Continued Access Study Patients
NCT01288586
Outcomes in Rotator Cuff Repair Using Graft Reinforcement
NCT01025037
Use of Graft Jacket for Rotator Cuff Repair
NCT00456781
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 3 | 1 |
Therapeutic Areas
What the Pipeline for Stryker Trauma and Extremities Shows
According to the ClinicalTrials.gov registry, Stryker Trauma and Extremities is linked to 30 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 7% of the sponsor's indexed portfolio, and 11 are already marked complete, representing roughly 37% of the total.
The phase mix for Stryker Trauma and Extremities reports 1 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Stryker Trauma and Extremities is Femoral Fracture with 3 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.
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.