Long Term Sidus PMCF
NCT04063943 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2021-05-13
Summary
The objectives of this study are to assess the safety and performance of the Sidus Stem-Free Shoulder Arthroplasty System in unilateral primary total shoulder arthroplasty.
Conditions
- Osteoarthritis
- Post-traumatic; Arthrosis
Interventions
- DEVICE
-
Sidus Stem-Free Shoulder
Device: Sidus Stem-Free Total Shoulder Arthroplasty System
Sponsors & Collaborators
-
Zimmer Biomet
lead INDUSTRY
Principal Investigators
-
Kacy Arnold, RN MBA · Zimmer Biomet
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-07-12
- Primary Completion
- 2020-01-31
- Completion
- 2020-03-31
- FDA Device
- Yes
Countries
- United States
- Canada
Study Locations
More Related Trials
-
DePuy Global Unite Shoulder System
NCT02412397 ·Status: UNKNOWN
-
INHANCE Stemless Reverse Shoulder IDE
NCT06323980 ·Status: RECRUITING ·Phase: NA
-
Long Term Follow-up of Integra® Cadence™ Total Ankle System in Primary Ankle Joint Replacement
NCT03247023 ·Status: TERMINATED
-
Clinical Evaluation of the Integra® Titan™ Modular Shoulder System Generation 2.5 for Primary Shoulder Joint Replacement
NCT03250767 ·Status: TERMINATED
-
This is a 2 Year Follow up Clinical and Radiographic Analysis of a Novel All Polyethelene Glenoid Component in Standard Total Shoulder Arthroplasty.
NCT01313741 ·Status: UNKNOWN ·Phase: PHASE4
-
Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder Arthroplasty
NCT01480453 ·Status: TERMINATED
-
GLOBAL ICON Stemless Shoulder System Post Market Clinical Follow Up Study
NCT03168672 ·Status: TERMINATED ·Phase: NA
-
Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder System
NCT01480440 ·Status: ACTIVE_NOT_RECRUITING
-
Post Market Clinical Follow-up (PMCF) Study of the A.L.P.S. Proximal Humerus Plating System
NCT03626038 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
To Evaluate the Safety and Clinical Radiological Outcomes in 2 Years of Embrance Model Reverse Shoulder Arthroplasty
NCT05569161 ·Status: RECRUITING
-
Multicenter Clinical Observation PROMOS®
NCT02280499 ·Status: COMPLETED
-
Perform Humeral System Study
NCT05067543 ·Status: RECRUITING
-
MDR - Comprehensive Primary Revision Stems PMCF
NCT06788717 ·Status: RECRUITING
-
PMCF Study of the CLS Brevius Stem With Kinectiv Technology
NCT03410940 ·Status: TERMINATED
-
Autologous Chondrocyte Implantation in the Patellofemoral Joint
NCT00212849 ·Status: COMPLETED
-
Comparison of Glenoid Position Using SmartBones
NCT03035318 ·Status: COMPLETED ·Phase: NA
-
One-stage Exchange Arthroplasty for Chronic Prosthetic Joint Infections
NCT03473392 ·Status: COMPLETED
-
Aequalis Resurfacing Head Study
NCT02444299 ·Status: UNKNOWN
-
A Study of Participants Undergoing Radial Head Replacement Using the DePuy Synthes Radial Head Replacement System for Partial Replacement of the Elbow Joint
NCT05415592 ·Status: WITHDRAWN
-
Post Market Clinical Follow-Up of the Zimmer Stafit Acetabular System
NCT04079114 ·Status: TERMINATED
-
MDR - Comprehensive Primary/Micro Stem & Versa-Dial Ti Humeral Head
NCT04003311 ·Status: ENROLLING_BY_INVITATION
-
Post-Approval Study of the R3 Biolox Delta Ceramic Acetabular System - Europe
NCT03566082 ·Status: COMPLETED
-
Long-term Study of The Press Fit Condylar (P.F.C.) Sigma Total Knee Replacement System
NCT00734110 ·Status: TERMINATED ·Phase: PHASE4
-
Arthrex Eclipse™ Shoulder Prosthesis
NCT01790113 ·Status: TERMINATED ·Phase: NA
-
Arthroplasty Cements Outcomes - A Post-market Follow-up
NCT06354543 ·Status: RECRUITING