Anderson, Allen |
NCT02123706: A Phase IIa, Single-blind, Placebo-controlled, Crossover, Multi-center, Randomized Study to Assess the Safety, Tolerability, and Preliminary Efficacy of a Single Intravenous Dose of Ischemia-tolerant Allogeneic Mesenchymal Bone Marrow Cells to Subjects With Heart Failure of Non-ischemic Etiology |
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| Recruiting | 2a | 20 | US | Human Allogeneic Mesenchymal Stem Cells, Mesenchymal Stem Cells, Marrow Stromal Cells, Placebo, Lactated Ringer's Solution | Stemedica Cell Technologies, Inc., CardioCell, LLC; A Stemedica Company | Non-ischemic Heart Failure | 06/16 | 06/16 | | |
| Recruiting | N/A | 870 | Canada, US | Edwards PASCAL System, Transcatheter tricuspid valve repair (TTVr), Optimal Medical Therapy | Edwards Lifesciences | Tricuspid Regurgitation, Tricuspid Valve Insufficiency, Tricuspid Valve Disease | 12/27 | 12/31 | | |
Kurtz, William B |
| Terminated | N/A | 49 | US | Conformis Hip System, Cordera Hip System | Restor3D | Clinical Condition Included in the Approved Indications For Use for the Conformis Hip System | 06/22 | 06/22 | | |
NCT04667559: A Study to Evaluate the Conformis iTotal Identity Knee Replacement System |
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| Terminated | N/A | 22 | US | Conformis iTotal Identity Knee Replacement System | Restor3D | Osteoarthritis, Knee | 12/22 | 12/22 | | |
Warren, Debbi |
NCT06741527: Integrity Implant System Post Market Clinical Follow-Up Study |
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| Not yet recruiting | 4 | 150 | US | Integrity Implant System | Anika Therapeutics, Inc. | Rotator Cuff Tears of the Shoulder | 06/27 | 10/27 | | |
CBDS, NCT05240755: Effectiveness of Cannabidiol vs. Narcotics for Post Operative Pain Control in Elective Shoulder Arthroscopic Surgery |
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| Recruiting | 1 | 50 | US | Cannabidiol Oil | Foundation for Orthopaedic Research and Education | Post-operative Pain | 02/25 | 12/25 | | |
NCT04012996: 2-level Cervical Disc Replacement Comparing Prodisc C SK & Vivo to Mobi-C |
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| Recruiting | N/A | 390 | US | prodisc C SK and/or Vivo, Mobi-C Cervical Disc | Centinel Spine | Symptomatic Cervical Disc Disease | 01/23 | 02/28 | | |
| Recruiting | N/A | 200 | US | Lumbar Interbody Fusion | 3Spine, MCRA | Lumbar Spine Degeneration | 05/24 | 08/26 | | |
| Recruiting | N/A | 300 | US | OssDsign® Catalyst | OssDsign | Degenerative Disc Disease, Spinal Stenosis | 03/27 | 04/27 | | |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
| Recruiting | N/A | 20 | US | Axoguard HA+ Nerve Protector™ | Axogen Corporation | Recurrent Cubital Tunnel Syndrome, Recalcitrant Cubital Tunnel Syndrome | 12/26 | 12/26 | | |
| Terminated | N/A | 8 | US | Surgical Management of Neuroma | Axogen Corporation | Chronic Neuropathic Pain | 01/24 | 01/24 | | |
NCT06040827: A Multicenter, Postmarket Surveillance Study of Subjects With the Canary canturioTM te Tibial Extension |
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| Recruiting | N/A | 626 | US | Total Knee Arthroplasty | Canary Medical | Knee Osteoarthritis | 06/28 | 12/28 | | |
NCT05719935: The KinematX Midcarpal Total Wrist Arthroplasty Registry |
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| Recruiting | N/A | 50 | US | KinematX total wrist arthroplasty system | Extremity Medical | Scapholunate Advanced Collapse (SLAC), Scapholunate Crystalline Advanced Collapse (SCAC), Scaphoid, Trapezium, and Trapezoid Advanced Collapse (STTAC), Carpal Tunnel Syndrome (CTS), Kienbock's Disease of Adults, Radial Malunion, Ulnar Translocation, Post Traumatic Arthritis, Inflammatory Arthritis, Osteoarthritis, Scaphoid Non-union Advanced Collapse (SNAC) | 12/35 | 12/35 | | |
Small, John |
NCT06350981: Analgesic Requirement for Post-Operative Pain Control in TLIP Interbody Fusion |
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| Enrolling by invitation | 2/3 | 76 | US | Exparel, Bupivacain | Foundation for Orthopaedic Research and Education, Pacira Pharmaceuticals, Inc | Back Pain, Surgery-Complications, Narcotic Use, Physical Stress, Post Operative Pain | 01/25 | 03/25 | | |
NCT03118505: A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation for Posterolateral Fusion (PLF) Treatment of Multi-Level Degenerative Lumbosacral Spinal Conditions |
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| Active, not recruiting | N/A | 100 | US | Infuse Bone Graft, Medtronic DBM | Medtronic Spinal and Biologics | Multi-Level Degenerative Lumbosacral Spinal Conditions | 04/26 | 12/26 | | |
| Recruiting | N/A | 200 | US | Lumbar Interbody Fusion | 3Spine, MCRA | Lumbar Spine Degeneration | 05/24 | 08/26 | | |
NCT05438719: MOTUS Total Joint Replacement Investigational Device Exemption Study |
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| Active, not recruiting | N/A | 158 | US | MOTUS Total Joint Replacement | 3Spine | Lumbar Spine Degeneration | 06/25 | 06/28 | | |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
Pestano, Cecile |
| Recruiting | N/A | 1000 | US | Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Medtronic Spinal and Biologics, Medtronic Bakken Research Center | Spinal Deformity, Spinal Degenerative Disorder, Spinal Fusion Failure, Spinal Trauma, Spinal Tumor Case | 05/31 | 05/31 | | |
Rolfe, Rena Clayton |
| Terminated | N/A | 49 | US | Conformis Hip System, Cordera Hip System | Restor3D | Clinical Condition Included in the Approved Indications For Use for the Conformis Hip System | 06/22 | 06/22 | | |
NCT04667559: A Study to Evaluate the Conformis iTotal Identity Knee Replacement System |
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| Terminated | N/A | 22 | US | Conformis iTotal Identity Knee Replacement System | Restor3D | Osteoarthritis, Knee | 12/22 | 12/22 | | |
Foreman, Paul M |
PICASSO, NCT05611242: Proximal Internal Carotid Artery Acute Stroke Secondary to Tandem or Local Occlusion Thrombectomy Trial |
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| Recruiting | 3 | 404 | US | MT+CAS with IV-AP, Thrombectomy, MT+CAS with PO-AP, MT+CAT with PO-AP | Mercy Health Ohio | Acute Ischemic Stroke | 03/26 | 05/27 | | |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
Snowden, Ryan |
NCT05405374: OSTEOAMP Lumbar Fusion Intra-Patient Controlled Study |
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| Recruiting | N/A | 101 | US | OSTEOAMP, Infuse | Bioventus LLC | Lumbar Spine Disease, Lumbar Spondylolisthesis, Lumbar Spine Instability, Lumbar Spondylosis, Degenerative Disc Disease | 10/24 | 10/25 | | |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
| Recruiting | N/A | 1000 | US | Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Medtronic Spinal and Biologics, Medtronic Bakken Research Center | Spinal Deformity, Spinal Degenerative Disorder, Spinal Fusion Failure, Spinal Trauma, Spinal Tumor Case | 05/31 | 05/31 | | |
Khairi, Saad |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
Lemrick, Nicole |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
Fraizer, Erika |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
Frazier, Erika |
NCT05405374: OSTEOAMP Lumbar Fusion Intra-Patient Controlled Study |
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| Recruiting | N/A | 101 | US | OSTEOAMP, Infuse | Bioventus LLC | Lumbar Spine Disease, Lumbar Spondylolisthesis, Lumbar Spine Instability, Lumbar Spondylosis, Degenerative Disc Disease | 10/24 | 10/25 | | |
NCT04715139: Evaluate the Continued Safety and Performance of the Foot and Ankle Products |
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| Recruiting | N/A | 650 | Europe, US, RoW | Products listed in Group/Cohort Description | Arthrex, Inc. | Hyperpronated Foot, Reconstruction Surgeries of the Foot, Fixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/Ankle, Fixation of Small Bone Fragments of the Foot/Ankle, Lisfranc Arthrodesis, Mono or Bi-cortical Osteotomies in the Forefoot, First Metatarsophalangeal Arthrodesis, Akin Osteotomy, Midfoot and Hindfoot Arthrodeses or Osteotomies, Fixation of Osteotomies for Hallux Valgus Treatment (Scarf and Chevron), Arthrodesis of the Metatarsocuneiform Joint to Reposition and Stabilize Metatarsus Primus Varus, Osteotomy Fixation of Hallux Valgus Repair (Such as Scarf and Chevron Etc.) | 12/24 | 12/24 | | |
| Recruiting | N/A | 1000 | US | Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Medtronic Spinal and Biologics, Medtronic Bakken Research Center | Spinal Deformity, Spinal Degenerative Disorder, Spinal Fusion Failure, Spinal Trauma, Spinal Tumor Case | 05/31 | 05/31 | | |
Stuntebeck-Poff, Susan |
NCT03118505: A Study of Infuse® Bone Graft With Mastergraft® Strip and Posterior Fixation for Posterolateral Fusion (PLF) Treatment of Multi-Level Degenerative Lumbosacral Spinal Conditions |
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| Active, not recruiting | N/A | 100 | US | Infuse Bone Graft, Medtronic DBM | Medtronic Spinal and Biologics | Multi-Level Degenerative Lumbosacral Spinal Conditions | 04/26 | 12/26 | | |
| Recruiting | N/A | 1017 | US, RoW | Infuse™ Bone Graft (Infuse™), Intervertebral body fusion device and Medtronic posterior Fixation Systems | Medtronic Spinal and Biologics | Degenerative Disease of the Lumbosacral Spine | 04/26 | 04/28 | | |
McMains, Craig |
| Recruiting | N/A | 1000 | US | Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Medtronic Spinal and Biologics, Medtronic Bakken Research Center | Spinal Deformity, Spinal Degenerative Disorder, Spinal Fusion Failure, Spinal Trauma, Spinal Tumor Case | 05/31 | 05/31 | | |
McCarthy, Kathryn |
| Recruiting | N/A | 1000 | US | Follow-up schedule: pre-operative baseline up to 24-months post-procedure | Medtronic Spinal and Biologics, Medtronic Bakken Research Center | Spinal Deformity, Spinal Degenerative Disorder, Spinal Fusion Failure, Spinal Trauma, Spinal Tumor Case | 05/31 | 05/31 | | |