Clinical trials: Shoulder Prosthesis
Staphylococcal Infections, Methicillin-resistant Staphylococcus Aureus
Daptomycin Use for Antimicrobial Prophylaxis in Methicillin Resistant Staphylococcus Aureus (MRSA) Colonized Adult Patients Undergoing Primary Elective Hip, Knee, or Shoulder Arthroplasty
This study will evaluate the safety and effectiveness of daptomycin, an antibiotic compared to another one which is vancomycin when given around the time of joint replacement surgery.
- Trial name
- NCT01196169
- Testing
- Daptomycin, Vancomycin
- Where
- 2 sites in United States
- Volunteers
- 28 people
- Sponsor
- Mountain Home Research & Education Corporation
Shoulder Posterior Instability, Shoulder Anterior Instability
Evaluating Upper Limb Movement Precision With AuReha in People With One-Sided Motor Impairment
The clinical investigation is designed as a controlled, two-arm, intra-patient, non-randomized interventional study aimed at assessing the capabilities of the AuReha system in detecting upper limb movement precision in patients…
- Conditions
- Shoulder Posterior Instability, Shoulder Anterior Instability, Shoulder Anterior Latarjet Instability, Adhesive Capsulitis, Shoulder
- Trial name
- NCT07133100
- Testing
- Upper limb rehabilitation wearable device
- Where
- Italy
- Volunteers
- 52 people
- Sponsor
- DigitalRehab
Rotator Cuff Arthropathy
Prosthesis Versus Active Exercise Program in Patients With Rotator Cuff Arthropathy
Reverse shoulder arthroplasty (RSA) is a well-established treatment for rotator cuff arthropathy. However, the effectiveness of RSA has not been compared to non-surgical treatment in a randomised controlled trial.
- Trial name
- REACT (NCT04864158)
- Testing
- TSA-group, Exercise-group
- Where
- 8 sites in Denmark, Estonia and 2 more
- Volunteers
- 102 people
- Sponsor
- University of Aarhus
Implantation of a Reverse Shoulder Prosthesis
To Evaluate the Safety and Clinical Radiological Outcomes in 2 Years of Embrance Model Reverse Shoulder Arthroplasty
The use of inverted prostheses to replace shoulder joints damaged by degenerative or traumatic processes has become widespread over the past three decades.
- Trial name
- NCT05569161
- Where
- Spain
- Volunteers
- 250 people
- Sponsor
- Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal
Rotator Cuff Deficiency, Shoulder Arthropathy
Reverse Shoulder Prosthesis Prospective Multi-Center Study
The purpose of this study is to evaluate the use and efficacy of the Reverse® Shoulder Prosthesis for treatment of rotator cuff deficiency in subjects who are candidates for a total shoulder replacement (primary and revision…
- Conditions
- Rotator Cuff Deficiency, Shoulder Arthropathy, Failed Shoulder Replacement
- Trial name
- NCT01005446
- Testing
- Encore Reverse Shoulder Prosthesis (RSP®)
- Where
- 10 sites in United States
- Volunteers
- 245 people
- Sponsor
- Encore Medical, L.P.
Revision of a Shoulder Prosthesis
PMCF Study on the Safety, Performance and Clinical Benefits Data of the Anatomical Shoulder Bipolar System
The study is a monocentric, retrospective and prospective, non-randomized, non-controlled and consecutive series post-market study.
- Trial name
- NCT05358574
- Where
- Germany
- Volunteers
- 40 people
- Sponsor
- Zimmer Biomet
Shoulder Arthroplasty, Shoulder Joint Disease
Radiographic and Clinical Outcomes After Short-Stem Reverse Shoulder Arthroplasty
Reverse total shoulder arthroplasty (RTSA) has become increasingly common in recent years due to expanding indications and improved surgical techniques.
- Conditions
- Shoulder Arthroplasty, Shoulder Joint Disease, Reverse Shoulder Prosthesis
- Trial name
- STEP2yrs (NCT07651215)
- Where
- Austria
- Volunteers
- 50 people
- Sponsor
- Krankenhaus Barmherzige Schwestern Linz
Massive Rotator Cuff Tears, Shoulder Disease
Effectiveness of Treatments for Massive Rotator Cuff Tears: Mixed Methodology.
The purpose of this study is: 1) to identify relevant treatment outcomes for people with massive rotator cuff tears of the shoulder joint, according to the experience of the affected people, to facilitate treatment shared…
- Trial name
- NCT05780229
- Testing
- Conservative treatment, Arthroscopic Decompression Surgery, Reverse Prosthesis
- Where
- 6 sites in Spain
- Volunteers
- 200 people
- Sponsor
- Parc de Salut Mar
Rotator Cuff Deficiency, Glenohumeral Arthritis
Retrospective Encore Reverse Shoulder Prosthesis Study
The purpose of this study is to evaluate the survivorship and efficacy of the Encore Reverse Shoulder Prosthesis in a group of no more than 50 subjects for whom data collection has already begun.
- Trial name
- NCT00765037
- Testing
- Encore Reverse Shoulder Prosthesis
- Where
- United States
- Volunteers
- 19 people
- Sponsor
- Encore Medical, L.P.
Glenohumeral Osteoarthritis
Poly vs Hybrid Glenoid in Stemless aTSA
Participants are randomized 1:1 to receive either a cemented all-polyethylene pegged glenoid or a hybrid trabecular titanium-pegged glenoid during anatomic total shoulder arthroplasty.
- Trial name
- Poly vs hybrid (NCT07520721)
- Testing
- Anatomic total shoulder arthroplasty with cemented all-polyethylene pegged glenoid, Anatomic total shoulder arthroplasty with hybrid trabecular titanium central-peg glenoid
- Where
- Netherlands
- Volunteers
- 94 people
- Sponsor
- Spaarne Gasthuis
Outcomes Assessments, Patients, Rotator Cuff Arthropathy
Influenze of Approach in Reversed Shoulder Prosthesis
To determine the differences in the placement of the glenoid implant of the inverted prostheses when they are implanted using a superior approach and using an anterior approach.
- Trial name
- NCT04405947
- Testing
- Reverse Shoulder Arthroplasty
- Volunteers
- 100 people
- Sponsor
- Hospital del Mar
Pain, Postoperative
Pain Management After Shoulder Prosthesis: A Clinical Trial of Nerve Block and Local Infiltration
The purpose of this study is to determine the efficacy of local infiltration analgesia as compared to 48-hour interscalene block in treating pain after shoulder arthroplasty.
- Trial name
- NCT01362075
- Testing
- Local infiltration analgesia, Interscalene catheter
- Where
- 2 sites in Denmark
- Volunteers
- 74 people
- Sponsor
- Horsens Hospital
Humeral Fracture, Proximal, Glenohumeral Osteoarthritis
RETRO-PROSPECTIVE POSTMARKET CLINICAL STUDY FOR FX SHOULDER SOLUTIONS SHOULDER SYSTEMS
This study takes place in the framework of the PostMarket Clinical Follow-up plan of the Shoulder Systems commercialized by FX SHOULDER SOLUTIONS. The included cases will be followed for 10 years after index surgery.
- Conditions
- Humeral Fracture, Proximal, Glenohumeral Osteoarthritis, Avascular Necrosis of the Head of Humerus, Rotator Cuff Tear
- Trial name
- NCT07558590
- Testing
- Shoulder arthroplasty
- Where
- 22 sites in France, Monaco
- Volunteers
- 1,004 people
- Sponsor
- FX Solutions
Shoulder Prosthesis
Prosthetic Component Relationship of the Reversed Delta III Total Shoulder Prosthesis in the Transverse Plane of the Body
Comparison of the function and mobility of the shoulder with the placement of the Delta prosthesis (anteversion and retroversion of the glenoidal and humeral components)
- Trial name
- NCT00284401
- Testing
- Evaluation of the placement of the Delta prosthesis
- Where
- Belgium
- Volunteers
- 50 people
- Sponsor
- University Hospital, Ghent
Osteoarthritis of the Shoulder, Proximal Humeral Fracture
Functional Outcome and Complications After Global Unite ® Prostheses
This study aims to investigate the shoulder function of patients with osteoarthritis or a fracture of the upper extremity after surgery with the Global Unite shoulder system.
- Trial name
- NCT03097406
- Testing
- Global Unite hemiarthroplasty, Global Advantage, Global FX
- Where
- 2 sites in Denmark
- Volunteers
- 88 people
- Sponsor
- Herlev and Gentofte Hospital
Osteoarthritis
A Trial Between the Intra-articular Local Anesthetic Infiltration With Catheter and Interscalene Block With Catheter in Postoperative Analgesia After Shoulder Prosthesis
The control of perioperative pain is necessary to avoid worst surgical suites after shoulder arthroplasty. Interscalene block (ISB) with or without catheter is the gold standard in postoperative analgesia after shoulder…
- Trial name
- LIA (NCT02365181)
- Testing
- intra-articular local anesthetic infiltration, inter-scalene block, Ropivacaine 2 %
- Where
- 5 sites in France
- Volunteers
- 98 people
- Sponsor
- Hospital Ambroise Paré Paris
Idiopathic Osteoarthritis, Posttraumatic Osteoarthritis
Humeral Head Implants: Radiological and Clinical Evaluation
In the past years several shoulder reconstruction systems with different types of prostheses and fixation methods have been developed to improve shoulder arthroplasty, trying to cover a wide range of pathologies and revision…
- Conditions
- Idiopathic Osteoarthritis, Posttraumatic Osteoarthritis, Humeral Head Necrosis, Instability Arthritis
- Trial name
- NCT02754024
- Testing
- Total shoulder arthroplasty (TSA), Hemi shoulder arthroplasty (HSA), Eclipse™ (Arthrex Inc., Naples, FL, USA)
- Volunteers
- 100 people
- Sponsor
- Werner Anderl
Reverse Shoulder Prosthesis
An Algorithm Creation by Automated Segmentation by MRI for Bone and Muscles of Shoulder
The primary objective of the study is to develop an algorithm of automated segmentation of shoulder by MRI examinations.
- Trial name
- SEGMENTATION (NCT05376813)
- Testing
- CT-Scan and MRI
- Volunteers
- healthy volunteers welcome
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Cuff Tear Arthropathy, Osteoarthritis With Cuff Deficiency
Long-term Clinical Effectiveness of the Delta Xtend Reverse Total Shoulder
This post-marketing study is designed to collect data relating to the use of the Delta Xtend™ Total Shoulder Replacement System in shoulder with rotator cuff deficiencies.
- Conditions
- Cuff Tear Arthropathy, Osteoarthritis With Cuff Deficiency, Rheumatoid Arthritis, Post Traumatic Injury to Shoulder
- Trial name
- NCT00737087
- Testing
- Delta Xtend Reverse Total Shoulder
- Where
- 5 sites in Belgium, France and 1 more
- Volunteers
- 144 people
- Sponsor
- DePuy International
Primary or Secondary Omarthrosis of the Shoulder Joint
Patient Benefit From the New Modular Shoulder Prosthesis PROMOS
Overall study design: This study is a prospective, non-randomized, multicenter postmarket clinical follow-up study with two study arms using the two shoulder prosthesis PROMOS™ STANDARD (group A) and PROMOS REVERSE™ (group B).
- Trial name
- Promos (NCT00925496)
- Where
- 2 sites in Germany, Switzerland
- Volunteers
- 155 people
- Sponsor
- Smith & Nephew Orthopaedics AG