Stryker: all 245 studies

Page 2 of 3. Open to participants first (22), then studies with results posted, then the rest; newest registration first within each.

• Secur-Fit Advanced Outcomes StudyTerminatedNCT01917929Not applicableResults posted
• BioFiber Scaffold Post-Market Observational StudyCompletedNCT01849458Results posted
• Phase II Study of the Effects of rhPDGF-BB Injection on Lateral EpicondylitisCompletedNCT01746420Phase 2Results posted
• Safety and Effectiveness of an Intracranial Aneurysm Embolization System for Treating Large or Giant Wide Neck AneurysmsCompletedNCT01716117Not applicableResults posted
• Trans-Nasal Maxillary Multi-Sinus Balloon Dilation StudyCompletedNCT01612780Not applicableResults posted
• Perfusion Assessment in Laparoscopic Left Anterior ResectionCompletedNCT01560377Phase 1Results posted
• XprESS Maxillary Balloon Dilation StudyCompletedNCT01525862Not applicableResults posted
• Randomized Evaluation of Maxillary Antrostomy Versus Ostial Dilation Efficacy Through Long-Term Follow-UpCompletedNCT01525849Not applicableResults posted
• Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System StudyTerminatedNCT01420237Not applicableResults posted
• Simpliciti IDE Trial; Replacing the Humeral Head in Total Shoulder ArthroplastyCompletedNCT01390038Phase 3Results posted
• Acellular Porcine Dermal Matrix Wound Dressing in the Management of Diabetic Foot UlcersCompletedNCT01353495Not applicableResults posted
• MiDAS III (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation StudyCompletedNCT01315145Not applicableResults posted
• Pelvic Alignment Level (PAL) Instrument EvaluationTerminatedNCT01312428Not applicableResults posted
• Augment® Injectable Bone Graft Compared to Autologous Bone Graft as a Bone Regeneration Device in Hindfoot FusionsCompletedNCT01305356Not applicableResults posted
• A Prospective, Post-market, Multi-center Feasibility Study of the BioDuct® Meniscal Repair DeviceTerminatedNCT01270919Not applicableResults posted
• Randomized Trial Evaluating Performance of the Trevo Retriever Versus the Merci Retriever in Acute Ischemic StrokeCompletedNCT01270867Not applicableResults posted
• Rejuvenate Modular Outcomes StudyCompletedNCT01257568Not applicableResults posted
• Safety and Effectiveness of the Adherus Dural Sealant System When Used as a Dural Sealant in Cranial ProceduresCompletedNCT01158378Phase 3Results posted
• XprESS Registry StudyCompletedNCT01115309Not applicableResults posted
• Thrombectomy REvascularization of Large Vessel Occlusions in Acute Ischemic Stroke (TREVO)CompletedNCT01088672Phase 4Results posted
• MiDAS II (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation StudyCompletedNCT01082159Phase 4Results posted
• Tritanium® Primary Acetabular Shell StudyTerminatedNCT01063751Not applicableResults posted
• Outcomes in Rotator Cuff Repair Using Graft ReinforcementCompletedNCT01025037Not applicableResults posted
• Healthcare Utilization and Outcomes of FinESS Treatment in the OfficeCompletedNCT00986830Not applicableResults posted
• Triathlon® Partial Knee Replacement (PKR) Outcomes StudyTerminatedNCT00966979Not applicableResults posted
• Scorpio® Cruciate Retaining (CR) Outcomes StudyTerminatedNCT00965146Not applicableResults posted
• Restoration® Modular Revision Hip System Post Market StudyCompletedNCT00962013Not applicableResults posted
• ABC/Trident® Ceramic Post Approval StudyCompletedNCT00960206Not applicableResults posted
• Triathlon Total Stabilizer (TS) Outcomes StudyCompletedNCT00958789Not applicableResults posted
• Omnifit Hydroxylapatite (HA) Hip Outcomes StudyTerminatedNCT00958347Not applicableResults posted
• Trident® X3 Polyethylene Insert StudyCompletedNCT00958191Not applicableResults posted
• Triathlon® Cruciate Retaining (CR) Total Knee System Outcomes StudyCompletedNCT00957723Not applicableResults posted
• Accolade® TMZF® Hip Stem Outcomes StudyCompletedNCT00957658Not applicableResults posted
• Triathlon® Posteriorly Stabilized (PS) Total Knee System - Outcomes StudyCompletedNCT00957021Not applicableResults posted
• MiDAS I (Mild® Decompression Alternative to Open Surgery): Vertos Mild Patient Evaluation StudyCompletedNCT00956631Phase 4Results posted
• An International Registry of the Wingspan™ Stent System for the Treatment of Intracranial Atherosclerotic StenosisCompletedNCT00929383Results posted
• The Vertos MILD™ Preliminary Patient Evaluation StudyCompletedNCT00749073Not applicableResults posted
• Balloon REmodeling Antrostomy THErapy StudyCompletedNCT00645762Phase 2Results posted
• Augment® Bone Graft (Formerly GEM OS™1 Bone Graft) Compared to Autologous Bone Graft in Foot and Ankle FusionsCompletedNCT00583375Not applicableResults posted
• Trident® Tritanium™ Acetabular Shell Revision StudyCompletedNCT00535626Not applicableResults posted
• LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert StudyCompletedNCT00510458Not applicableResults posted
• Evaluation of Triathlon - a New Total Knee Prosthesis System - Triathlon vs. DuraconCompletedNCT00436982Not applicableResults posted
• MAPS Trial: Matrix And Platinum ScienceCompletedNCT00396981Phase 4Results posted
• Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow UpActive, not recruitingNCT07245810
• Facial iD Customized Mandible Reconstruction PlatesCompletedNCT07245758
• Stryker Universal Midface and Upper-Face Fixation System: A Retrospective Post Market Follow UpCompletedNCT07245719
• Stryker's Surgeon iD Mandible Reconstruction Plates: A Retrospective Post Market Follow UpCompletedNCT07221916
• Retrospective Study of Suture Tape for Soft Tissue Reconstruction in Patients Suffering From Lateral Ankle InstabilityCompletedNCT06829667
• Study of Artelon FLEXBAND® for Patients Undergoing Soft Tissue Reconstruction of the Anterior Talofibular Ligament (ATFL) to Treat Lateral Ankle InstabilityCompletedNCT06638138Not applicable
• The Protrieve PROTECTOR StudyCompletedNCT06495996Not applicable
• Amplitude Vascular Systems (AVS) Lithotripsy POWER PAD 2 TrialActive, not recruitingNCT06457685Not applicable
• Evolve China PMCF StudyActive, not recruitingNCT06368622
• Blueprint® Mixed Reality Pilot StudyCompletedNCT06080412
• The PEERLESS II StudyActive, not recruitingNCT06055920Not applicable
• Shoulder iD™ Primary Reversed Glenoid Outcomes Clinical StudyActive, not recruitingNCT05868148
• Perform® Humeral System - Fracture Study (PFX)Active, not recruitingNCT05773352
• Restoration Anatomic Acetabular Shell Revision StudyWithdrawnNCT05591859Not applicable
• China Surpass Streamline Post-Market StudyTerminatedNCT05544045
• Post Market Clinical Evaluation of Gamma 4CompletedNCT05523635
• Stryker PEEK Customized Implant: A Prospective Post Market Follow Up to Evaluate Safety, Performance and EffectivenessActive, not recruitingNCT05362370
• POWER: Pulse Intravascular Lithotripsy (Pulse IVL) to Open Vessels With Calcific Walls and Enhance Vascular Compliance and RemodelingActive, not recruitingNCT05192473Not applicable
• Insignia™ Hip Stem Outcomes StudyActive, not recruitingNCT05144191Not applicable
• Pyrocarbon Clinical Follow-up StudyActive, not recruitingNCT05049993
• SPY Fluorescence Imaging Systems and Indocyanine Green to Determine the Percentage of Successful Critical Anatomy Recognition in Laparoscopic Cholecystectomy Surgeries.TerminatedNCT05006950Phase 1
• US IDE Study of the Contour NEurovasCular System™ for IntraCranial Aneurysm RepairActive, not recruitingNCT04852783Phase 4
• SpineJack System Postmarket RegistryCompletedNCT04795765
• Triathlon All-Polyethylene Tibia Outcomes StudyActive, not recruitingNCT04636190Not applicable
• A Trial of Mechanical Axis With Soft Tissue Release Balancing vs Functional Alignment With Bony Release Balancing in Total Knee Replacement Using Stryker's Mako RobotActive, not recruitingNCT04600583Not applicable
• INFINITY™ With ADAPTIS™ Technology StudyActive, not recruitingNCT04594993
• Post Market Clinical Follow-up (PMCF)Study of the Contour Neurovascular SystemTMWithdrawnNCT04579081
• International Post Market Surveillance Study of Intracranial Aneurysms Treated With an Endovascular ApproachActive, not recruitingNCT04572230
• Effectiveness and Safety of LED Light Source System for EndoscopeWithdrawnNCT04561583Not applicable
• Objective to Evaluate the Safety and Effectiveness of LED Light Source System for Endoscopy in Ureteral RadiographyWithdrawnNCT04561414Not applicable
• Trenza Embolization Device for Intrasaccular Aneurysm TreatmentCompletedNCT04380350
• Natural Progression of High-Risk Chronic Limb-Threatening Ischemia: The CLariTI StudyCompletedNCT04304105
• Evaluation of Safety and Effectiveness of Stryker Surpass Evolve™ Flow Diverter SystemActive, not recruitingNCT04195568Not applicable
• Elbow Outcomes Clinical Study (WELBOW)CompletedNCT04173377
• Safety and Performance of the Neuroform Atlas™ Stent SystemStatus unknownNCT04162483
• XprESS ET RegistryCompletedNCT04136977
• Evaluation of Zip Device to Conventional Sutures for Laceration Repair in Pediatrics in an Emergency DepartmentStatus unknownNCT04122859Not applicable
• Citadel Embolization Device StudyActive, not recruitingNCT04057352Not applicable
• Collecting Orthopedic Safety and Performance Data Using Surgeons Clinical Outcomes Registry (SCOR)TerminatedNCT04032444
• A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the Femoral Nail PFCompletedNCT04015154
• A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the Femoral Nail GTCompletedNCT04015128
• Long-term Safety and Effectiveness of AUGMENT® Injectable Bone Graft Compared to Autologous Bone GraftStatus unknownNCT03998137
• Registry of Subject Treated With ClariFixCompletedNCT03739216
• Low Energy Dissection Vs. Electrocautery in Lumpectomy Shaved Surgical MarginsStatus unknownNCT03718442
• Post-op Outcomes of Enhanced Energy Delivery Dissection for Mastectomy With Immediate Breast ReconstructionStatus unknownNCT03627442Not applicable
• ZipLine Incision Approximation Verses Suture:ZIPS3 Physician Preference StudyWithdrawnNCT03201536Not applicable
• A Randomized Post-market Study to Evaluate Zip Device Compared to Sutures for Laceration Repair in Pediatrics and AdultsCompletedNCT03199456Not applicable
• Evaluation of Triathlon - A New Total Knee Prosthesis System - Triathlon PA vs. Triathlon PressfitCompletedNCT03198533Not applicable
• UK Infinity, Post-Market Clinical Follow-up StudyActive, not recruitingNCT03063593
• Trident II Tritanium Acetabular Shell Outcomes StudyActive, not recruitingNCT02999009Not applicable
• Zip Incision Approximation vs. Suture for C-SectionStatus unknownNCT02915952Not applicable
• ENRICH: Early MiNimally-invasive Removal of IntraCerebral Hemorrhage (ICH)CompletedNCT02880878Not applicable
• Long-term Safety and Effectiveness of AUGMENT® Bone Graft Compared to Autologous Bone GraftStatus unknownNCT02879149
• Neuroform Atlas Stent for Intracranial Aneurysm TreatmentCompletedNCT02783339
• Post Market Clinical Follow Up Study for Evaluation of Agluna® METSCompletedNCT02779504
• The Evaluation of the METS™ Proximal Humeral SystemCompletedNCT02774174
• SpineJack® Versus Conservative Treatment Study (SPICO Study)CompletedNCT02657265Not applicable

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