Clinical trials: Arthroplasty Shoulder
Glenohumeral Osteoarthritis
Pyrocarbon Hemiarthroplasty Versus Total Shoulder Arthroplasty for the Treatment of Glenohumeral Osteoarthritis
This is a multi-center study assessing postoperative outcomes associated with hemiarthroplasty with pyrocarbon (hPYC) versus anatomic total shoulder arthroplasty (aTSA).
- Trial name
- NCT07226388
- Testing
- Hemiarthroplasty with pyrocarbon, Anatomic total shoulder arthroplasty
- Where
- United States
- Volunteers
- 74 people
- Sponsor
- Washington University School of Medicine
Shoulder Arthroplasty, Postoperative Pain
Superior Trunk Block Catheter Versus Single-shot Superior Trunk Block With Intravenous Dexmedetomidine for Shoulder Arthroplasty
Shoulder arthroplasty is associated with significant postoperative pain. Appropriate pain control after shoulder arthroplasty is crucial for postoperative rehabilitation and patient satisfaction.
- Trial name
- NCT05020821
- Testing
- Single-shot superior trunk block with intravenous dexmedetomidine, Continuous superior trunk block
- Where
- South Korea
- Volunteers
- 92 people
- Sponsor
- Yonsei University
Shoulder Arthroplasty
Comparison of Conventional, Patient-Specific, and Augmented Reality Navigation in Reverse Total Shoulder Arthroplasty
This monocentric observational cohort study compares conventional instrumentation, patient-specific instrumentation, and augmented reality navigation in reverse total shoulder arthroplasty.
- Trial name
- STEP-AR (NCT07645508)
- Where
- Austria
- Volunteers
- 50 people
- Sponsor
- Krankenhaus Barmherzige Schwestern Linz
Analgesia
Liposomal Bupivacaine Versus Non-liposomal Bupivacaine for Total Shoulder Arthroplasty
The objective of this study is to validate the analgesic efficacy of admixed Liposomal bupivacaine (LB) + bupivacaine compared with plain bupivacaine when injected for interscalene nerve block (ISNB) for total shoulder…
- Trial name
- NCT04974385
- Testing
- Liposomal bupivacaine, Bupivacaine
- Where
- United States
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- University of Virginia
Fracture
Anatomical Shoulder™ Fracture PMCF Study
The purpose of this study is to obtain outcomes data on the Anatomical Shoulder Fracture System by analysis of standard scoring systems and radiographs.
- Trial name
- NCT02465398
- Testing
- Fracture Shoulder Arthroplasty
- Where
- 3 sites in Germany, Switzerland and 1 more
- Volunteers
- 52 people
- Sponsor
- Zimmer Biomet
Reverse Shoulder Replacement
Tornier Blueprint Planning Software in Patients Receiving Reverse Shoulder Arthroplasty
Compare sizing determined in pre-operative planning of reverse shoulder arthroplasty to operative implant size selected.
- Trial name
- NCT04474665
- Testing
- Reverse shoulder arthroplasty utilizing Blueprint Software
- Where
- United States
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Spine Institute of Louisiana Foundation
Rheumatic Disease
Immunosuppressant Management in Rheumatology Patients Undergoing Elective Total Shoulder Arthroplasty
The purpose of this study is to assess the incidence of rheumatologic flares, changes in pain scores (VAS), changes in functional outcomes (PROMIS), wound complications, surgical site infections, and return trips to the operating…
- Trial name
- NCT07138898
- Testing
- Methotrexate, Sulfasalazine, Hydroxychloroquine
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- NYU Langone Health
Total Shoulder Arthroplasty
Postoperative Pain Control in Total Shoulder Arthroplasty
A double blind, prospective, randomized trial to evaluate postoperative pain, narcotic use, patient satisfaction, and function among shoulder arthroplasty patients receiving interscalene block with and without the addition of…
- Trial name
- NCT05068960
- Testing
- Liposomal bupivacaine, Bupivacaine
- Where
- United States
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Scripps Clinic
Opioid Use
Opioid Consumption and Disposal After Shoulder Arthroplasty
Opioid medications are widely used after many orthopedic procedures and are routinely prescribed after shoulder replacement surgery.
- Trial name
- NCT05525975
- Testing
- Educational materials
- Where
- United States
- Volunteers
- 140 people, healthy volunteers welcome
- Sponsor
- Brendan M. Patterson
Glenohumeral Osteoarthritis
Comparison of Stemless and Stemmed Shoulder Arthroplasty for Osteoarthritis
This is a randomized controlled trial comparing the Comprehensive Nano stemless total shoulder arthroplasty (intervention group) with the Comprehensive un-cemented stemmed total shoulder arthroplasty (control group).
- Trial name
- NCT04105478
- Testing
- Shoulder arthroplasty
- Where
- Denmark
- Volunteers
- 122 people
- Sponsor
- Herlev and Gentofte Hospital
Arthropathy Shoulder
The Role of Subscapularis Repair in Reverse Shoulder Arthroplasty
The overall goal of the study is to determine if repairing the subscapularis tendon during primary reverse shoulder arthroplasty effects short-term patient outcomes.
- Trial name
- NCT03727490
- Testing
- Repair, Standard Treatment
- Where
- United States
- Volunteers
- 102 people, healthy volunteers welcome
- Sponsor
- Washington University School of Medicine
Arthroplasty Complications
Validation and Feasibility in Clinical Practice and Concordance of an Automated System Coupling an RGB-D Camera and a Software Based on Artificial Intelligence for the Measurement of Shoulder Range of Motion for Patients Operated on a Total Reversed Shoulder Prosthesis.
The functional evaluation of the shoulder, which is the most mobile joint in the human body, is a complex clinical examination to perform.
- Trial name
- NCT05292157
- Testing
- shoulder arthroplasty
- Where
- France
- Volunteers
- 30 people
- Sponsor
- Centre Hospitalier Universitaire de Nice
Shoulder Osteoarthritis
Subscapularis Strength After Total Shoulder Arthroplasty
This is a randomized, double-blinded, standard of care-controlled clinical trial. The purpose of this study is to determine the difference in subscapularis strength and function after anatomic Total Shoulder Arthroplasty (aTSA)…
- Trial name
- NCT03854357
- Testing
- Subscapularis Rehabilitation, Standard Rehabilitation
- Where
- United States
- Volunteers
- 66 people, healthy volunteers welcome
- Sponsor
- Henry Ford Health System
Surgical Wound, Shoulder Arthritis
Dermabond PRINEO for Total Shoulder Arthroplasty
This is a research study to find out whether wound closure (the process of closing the surgical wound after the procedure is complete) with Dermabond PRINEO Skin Closure System (PRINEO) will be faster and improve wound healing…
- Conditions
- Surgical Wound, Shoulder Arthritis, Surgical Incision
- Trial name
- NCT03860181
- Testing
- Subcuticular Sutures - Surgeon 1, Metal Staples - Surgeon 2, PRINEO - Surgeon 1
- Where
- United States
- Volunteers
- 89 people
- Sponsor
- Medical University of South Carolina
Shoulder Disease
Diaphragm-sparing Nerve Blocks for Shoulder Arthroplasty
The combination of a modified lateral sagittal infraclavicular block and a suprascapular nerve block has not been studied in a cohort of total arthroplasty patients.
- Trial name
- NCT03877835
- Testing
- Peripheral nerve blocks
- Where
- Norway
- Volunteers
- 20 people
- Sponsor
- University Hospital of North Norway
Glenohumeral Osteoarthritis
Anatomic Versus Reverse Shoulder Arthroplasty for Primary Glenohumeral Osteoarthritis
The primary goal of the investigators prospective randomized study is to determine whether reverse total shoulder arthroplasty (RTSA) have at least as good results as anatomic TSA (non-inferiority), in patients with glenohumeral…
- Trial name
- NCT06513559
- Testing
- Anatomic total shoulder replacement, Reverse total shoulder replacement
- Where
- United States
- Sponsor
- University of Utah
Shoulder Disease, Rotator Cuff Tear Arthropathy
Sling vs No Sling After Reverse Total Shoulder Arthroplasty
This study involves patients who will be undergoing a reverse total shoulder replacement at Duke University. 100 eligible will be randomly assigned into one of two groups, a sling or no sling group.
- Conditions
- Shoulder Disease, Rotator Cuff Tear Arthropathy, Shoulder Osteoarthritis
- Trial name
- NCT06092996
- Testing
- Time of Sling Use
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Duke University
Technology, Comparison
Comparison Between Exactech Guided Personalized Surgery (GPS) and Conventional Instrumentation of Shoulder Arthroplasty
The primary objective of this study is to examine the optimization of Reverse Shouder Arthroplasty implant position between GPS and conventional techniques.
- Trial name
- NCT05615259
- Where
- 2 sites in Netherlands
- Volunteers
- 260 people
- Sponsor
- Exactech
Shoulder Disease
Proximal Humerus Reconstruction After Resection for Tumors : Comparison Between Allograft Prosthetic Composite and Cement Sleeve Prosthetic Composite
Proximal humerus is a common site for primary bone tumors and metastatic disease. Reconstruction with reverse shoulder arthroplasty (RSA) after resection is a surgical challenge and presented high risk of complication.
- Trial name
- NCT06382779
- Testing
- reverse shoulder arthroplasty
- Where
- France
- Volunteers
- 32 people
- Sponsor
- Central Hospital, Nancy, France
Opioid Use
Opioid Use in Shoulder Arthroplasty Patients: A Stratification and Algorithm
The investigators aim to better understand opioid use in patients undergoing elective shoulder surgery. The investigators will prospectively determine actual postoperative opioid use, while evaluating whether implementation of an…
- Trial name
- NCT03808025
- Testing
- opioid education
- Where
- United States
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- University of California, Davis