Clinical trials: Shoulder Arthritis Osteoarthritis
Osteoarthritis
Effectiveness of Hemi- Versus Total Shoulder Arthroplasty Using Implants of the "Epoca" System
The clinical question on whether or not to replace the glenoid component in patients with a degenerative shoulder disease, has not been answered yet in a randomized study with enough statistical power.
- Trial name
- Epoca H vs T (NCT01288066)
- Testing
- Hemiarthroplasty, Total arthroplasty
- Where
- 4 sites in Austria, Germany and 1 more
- Volunteers
- 76 people
- Sponsor
- AO Innovation Translation Center
Rotator Cuff Syndrome of Shoulder and Allied Disorders, Osteoarthritis Shoulder
FX Shoulder Solutions Retrospective / Prospective Clinical Study
Subjects implanted with the shoulder replacement medical devices manufactured by FX Shoulder Solutions and distributed by FX Shoulder Solutions.
- Conditions
- Rotator Cuff Syndrome of Shoulder and Allied Disorders, Osteoarthritis Shoulder, Fracture, Shoulder
- Trial name
- NCT06077942
- Testing
- FX Artificial Shoulder Prosthesis
- Where
- 2 sites in United States
- Volunteers
- 600 people
- Sponsor
- FX Shoulder Solutions
Shoulder Osteoarthritis
Safety and Effectiveness of the Tornier Simpliciti™ Shoulder System in Shoulder Arthroplasty
The aim of this observationnal post-marketing study is to provide additional information on the safety and effectiveness of Simpliciti™ system at 24 months post-shoulder arthroplasty , in usual surgical practice.
- Trial name
- NCT02452957
- Where
- Germany
- Sponsor
- Stryker Trauma and Extremities
Shoulder Osteoarthritis
Effect of PRP as Therapy for Shoulder Osteoarthritis
Patients with shoulder osteoarthritis are suffering from pain and disabilities which lead to difficulties in life. The presence of platelet-rich plasma as regenerative therapy which helps in healing of damaged tissues like…
- Trial name
- NCT05043493
- Testing
- Injection in the intraarticular space of glenohumeral joint
- Where
- Egypt
- Volunteers
- 91 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Arthroplasty, Replacement, Shoulder, Glenoid Cavity
Long Term Follow-up After Primary or Revision Shoulder Arthroplasty With a Patient- Specific Glenius Implant
This post-market follow-up study investigates improvement in clinical and radiological outcome after reversed total shoulder arthroplasty with the patient-specific Glenius Glenoid Reconstruction system
- Conditions
- Arthroplasty, Replacement, Shoulder, Glenoid Cavity, Osteoarthritis of the Shoulder
- Trial name
- NCT03806881
- Testing
- reversed glenoid prothesis
- Where
- 4 sites in Belgium, Netherlands
- Volunteers
- 24 people
- Sponsor
- Materialise
Osteoarthritis, Osteoarthritis (OA) of the Knee
Systemic Oral Glucocorticoids for the Treatment of Acute Osteoarthritis Pain in the Emergency Department
The purpose of this clinical trial is to compare the analgesic effects (relief of pain) of glucocorticoids (steroids) and pain medication versus pain medication alone in adult patients presenting to the emergency department with…
- Conditions
- Osteoarthritis, Osteoarthritis (OA) of the Knee, Osteoarthritis (OA) of the Shoulder, Osteoarthritis (OA) of the Hip
- Trial name
- NCT06603662
- Testing
- Prednisone, Dexamethasone
- Where
- United States
- Volunteers
- 192 people
- Sponsor
- WellSpan Health
Osteoarthritis
Effectiveness of Manual Therapy and Exercise in Shoulder OA
Approximately 60 subjects from a sample of convenience diagnosed with shoulder arthritis will be randomized into a two groups. The control group will receive usual medical advice and the experimental group will be referred to…
- Trial name
- NCT02587559
- Testing
- physical therapy
- Where
- United States
- Sponsor
- University of Texas Southwestern Medical Center
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
Chronic Shoulder Pain
Treatment of Shoulder Osteoarthritis
The purpose of this study is to learn if pain can be relieved by delivering small amounts of electricity ("electrical stimulation") to the nerves relaying sensory information to the shoulder.
- Trial name
- NCT05657587
- Testing
- SPRINT PNS
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Gramercy Pain Center
Osteoarthritis Shoulder, Rotator Cuff Syndrome of Shoulder and Allied Disorders
FX Shoulder Prospective Clinical Study
Prospective Multi-Center Registry on study subjects with implanted devices marketed and legally commercialized in the USA by FX Shoulder Solutions.
- Conditions
- Osteoarthritis Shoulder, Rotator Cuff Syndrome of Shoulder and Allied Disorders, Fracture, Shoulder
- Trial name
- NCT06078865
- Testing
- FX Artificial Shoulder Prosthesis
- Where
- 4 sites in United States
- Volunteers
- 600 people
- Sponsor
- FX Shoulder Solutions
Cuff Tear Arthropathy, Primary Osteoarthritis
Follow-up Evaluating Clinical and Radiological Outcomes of Total Shoulder Arthroplasty With Permedica's MIRAI Prosthesis
This observational study is conducted in order to evaluate the effectiveness of the primary total shoulder arthroplasty with the Permedica's MIRAI Modular Shoulder Prosthesis System on the general population of patients who are…
- Conditions
- Cuff Tear Arthropathy, Primary Osteoarthritis, Secondary Osteoarthritis, Shoulder Osteoarthritis
- Trial name
- NCT05128500
- Testing
- Total Shoulder Arthroplasty with Permedica's MIRAI
- Where
- 4 sites in Germany, Italy and 1 more
- Volunteers
- 76 people
- Sponsor
- Permedica spa
Osteoarthritis Shoulder, Rotator Cuff Tears
DenCT Shoulder Bone Quality Evaluation
The objective of the study is to evaluate the preoperative bone quality assessment based on CT to later establish a scale for the decision of stemless shoulder arthroplasty.
- Trial name
- NCT06032416
- Testing
- Preoperative CT Scan
- Where
- Japan
- Volunteers
- 200 people
- Sponsor
- Zimmer Biomet
Cartilage Degeneration, Rotator Cuff Tear
Use of MRI Labeling Technique to Track Mesenchymal Stem Cell Survival in Orthopaedic Conditions
The primary objective is to determine whether a surgical intervention involving removing of the calcified cartilage cap in patients with Grade II Kellgren-Lawrence osteoarthritis influences the incorporation of labeled bone…
- Conditions
- Cartilage Degeneration, Rotator Cuff Tear, Osteoarthritis, Knee
- Trial name
- NCT03648463
- Testing
- arthroscopy of the affected knee/ Bone Marrow Concentrate Injection
- Sponsor
- Stanford University
Hip Osteoarthritis, Knee Osteoarthritis
Return to Golf After Orthopaedic Surgery
The GOLF study is a multicenter, prospective study with the goal to investigate golfers' return to the sport following hip, knee or shoulder arthroplasty.
- Conditions
- Hip Osteoarthritis, Knee Osteoarthritis, Shoulder Osteoarthritis
- Trial name
- NCT05675618
- Where
- 2 sites in United States, United Kingdom
- Volunteers
- 432 people
- Sponsor
- Hospital for Special Surgery, New York
Shoulder Osteoarthritis, Cuff Tear Arthropathy
Local Infiltration Analgesia Vs. Interscalene Block in Total Shoulder Arthorplasty
Pain management following total shoulder arthroplasty is an important factor in determining patient outcomes and satisfaction. Interscalene brachial plexus blockade has been used successfully to minimize pain in the acute…
- Conditions
- Shoulder Osteoarthritis, Cuff Tear Arthropathy, Massive Rotator Cuff Tear
- Trial name
- NCT04415931
- Testing
- Local infiltration analgesia, Interscalene block
- Where
- United States
- Volunteers
- 78 people
- Sponsor
- University of Missouri-Columbia
Total Shoulder Arthroplasty, Glenohumeral Osteoarthritis
A Retrospective Review of FloSeal Use in Total Shoulder Arthroplasty
The proposed study aims to objectively assess 2-year clinical and radiographic results for the rate of glenoid component loosening in total shoulder arthroplasty (TSA).
- Trial name
- NCT01726972
- Where
- United States
- Volunteers
- 41 people
- Sponsor
- Western Orthopaedics Research and Education Foundation
Osteoarthritis
Three Injections of EUFLEXXA (Sodium Hyaluronate) for Treatment of Chronic Shoulder Pain Associated With Osteoarthritis (OA)
The hypothesis of this study is that by using 3 injections of EUFLEXXA, there will be an improvement in pain levels and range of motion.
- Trial name
- NCT00969501
- Testing
- EUFLEXXA
- Where
- United States
- Volunteers
- 32 people
- Sponsor
- Georgia Institute for Clinical Research, LLC
Osteoarthritis, Shoulder Pain
Platelet-rich Plasma vs. Hyaluronic Acid for Glenohumeral Osteoarthritis
This study seeks to expand the current literature in demonstrating potentially efficacious, conservative treatments in the management of glenohumeral osteoarthritis (OA) and will compare ultrasound-guided injections of hyaluronic…
- Trial name
- NCT02984228
- Testing
- PRP, Hyaluronic Acid, Ultrasound
- Where
- United States
- Volunteers
- 70 people
- Sponsor
- Hospital for Special Surgery, New York
Orthopedic Disorder, Arthritis Shoulder
Blueprint® Mixed Reality Pilot Study
A pilot Single-Arm, Multicenter, Prospective, Post-Market 6 months Follow-Up Clinical Investigation to Evaluate the Safety and Effectiveness of the Blueprint Mixed Reality HOLOBLUEPRINT™ (HOLOBLUEPRINT™).
- Conditions
- Orthopedic Disorder, Arthritis Shoulder, Arthritis, Degenerative, Cuff Tear Arthropathy
- Trial name
- BLUEMR (NCT06080412)
- Where
- 4 sites in France
- Volunteers
- 44 people
- Sponsor
- Stryker Trauma and Extremities
Shoulder Arthroplasty, Shoulder Osteoarthritis
Programmed Intermittent Bolus During Continuous Interscalene Nerve Block for Shoulder Arthroplasty
A new infusion strategy named the 'programmed intermittent bolus' (PIB) technique delivers the hourly dose within minutes compared to the traditional infusion that delivers such dose over an hour.
- Conditions
- Shoulder Arthroplasty, Shoulder Osteoarthritis, Pain Management
- Trial name
- NCT03268837
- Testing
- Programmed Intermittent Bolus, Continuous Infusion
- Where
- Canada
- Volunteers
- 110 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's