Clinical trials: Arthroplasty Shoulder
Humeral Fracture, Proximal
Reverse Total Shoulder Arthroplasty Versus Hemiarthroplasty for Displaced 3- and 4-part Proximal Humeral Fractures
Proximal humeral fractures are common injuries with the highest incidence being amongst the elderly. Most proximal humeral fractures are nondisplaced or minimally displaced.
- Trial name
- NCT03383991
- Testing
- Reverse Total Shoulder Arthroplasty, Hemiarthroplasty
- Sponsor
- Karolinska Institutet
Osteoarthritis, Arthropathy
Liposomal Bupivacaine for Pain Control After Total Shoulder Arthroplasty
This study will compare interscalene nerve block versus liposomal bupivacaine (Exparel) for pain control after total shoulder replacements.
- Conditions
- Osteoarthritis, Arthropathy, Shoulder Pain, Closed Fracture Proximal Humerus, Four Part
- Trial name
- NCT02762071
- Testing
- Liposomal bupivacaine, Interscalene Nerve Block
- Where
- 2 sites in United States
- Volunteers
- 108 people
- Sponsor
- Johns Hopkins University
Shoulder Arthroplasty, Rehabilitation
Role of Nutritional Status in Functional Recovery of Older Adults Undergoing Virtual Reality-augmented Shoulder Rehabilitation (VIR)
Malnutrition is a clinical syndrome defined by involuntary weight loss and/or a persistent imbalance between nutritional needs and intake, leading to functional decline.
- Conditions
- Shoulder Arthroplasty, Rehabilitation, Virtual Reality, Malnutrition Elderly
- Trial name
- VIR (NCT07282561)
- Testing
- Oculus Quest
- Where
- Italy
- Volunteers
- 60 people
- Sponsor
- Claudio Pedone
Sleep Disturbance, Shoulder Arthritis
Multimodal Sleep Pathway for Shoulder Arthroplasty
The purpose of the study is to investigate the efficacy of sleep medicine in the recovery of orthopaedic shoulder arthroplasty patients.
- Conditions
- Sleep Disturbance, Shoulder Arthritis, Arthroplasty Complications, Perioperative/Postoperative Complications
- Trial name
- NCT03269760
- Testing
- Zolpidem
- Where
- United States
- Volunteers
- 122 people, healthy volunteers welcome
- Sponsor
- University of California, San Francisco
Proximal Humeral Fracture, Reverse Total Shoulder Arthroplasty
Duration of Immobilization After Reverse Total Arthroplasty for Proximal Humerus Fractures
The purpose of this study is to evaluate compare postoperative range of motion in patients who are given a sling for comfort only and allowed to start early active range of motion compared to patients who are placed in a sling…
- Trial name
- NCT06133920
- Testing
- Early Range of Motion, Immobilization
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- The Cooper Health System
Anesthesia, Local
Liposomal Bupivacaine Versus Bupivacaine for for Postoperative Pain Control in Shoulder Surgery
This is a randomized, single blinded clinical trial whose purpose is to assess the impact of liposomal bupivacaine (LB) in a single shot interscalene nerve block compared with standard bupivacaine (same dose) in a single shot…
- Trial name
- NCT04180943
- Testing
- interscalene nerve block
- Where
- United States
- Volunteers
- 85 people
- Sponsor
- Bassett Healthcare
Shoulder Arthroplasty
A Post-Market Clinical Evaluation of the ReUnion TSA System
This investigation is a prospective, multicenter clinical investigation. It is anticipated that a total of one hundred (100) subjects will be enrolled at approximately 4-7 sites.
- Trial name
- NCT03858517
- Testing
- ReUnion TSA System
- Where
- 3 sites in United States
- Volunteers
- 51 people
- Sponsor
- Stryker Trauma and Extremities
Shoulder Arthritis, Blood Loss, Surgical
Effect of TXA on Blood Loss in Reverse Total Shoulder Arthroplasty
Tranexamic acid (TXA) is a synthetic anti-fibrinolytic agent that has been well studied and routinely used for hip and knee arthroplasty.
- Conditions
- Shoulder Arthritis, Blood Loss, Surgical, Tranexamic Acid Adverse Reaction
- Trial name
- NCT06638749
- Testing
- Tranexamic Acid, Normal Saline
- Where
- United States
- Sponsor
- University of Kansas Medical Center
Shoulder Injuries
Increased Home-based Physical Therapy Adherence Using BAND Connect's VirtuaCare™ Platform
This study aims to enhance at-home therapy by introducing a new device called the BAND Connect's VirtuaCare™ platform. The study aims to determine whether patients can improve their adherence to at-home exercises using this…
- Trial name
- NCT05876208
- Testing
- BAND Connect's VirtuaCare™ platform, Standard of Care Physical Therapy
- Where
- United States
- Volunteers
- 77 people
- Sponsor
- University of Cincinnati
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
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, Post-traumatic; Arthrosis
Long Term Sidus PMCF
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.
- Trial name
- NCT04063943
- Testing
- Sidus Stem-Free Shoulder
- Where
- 7 sites in United States, Canada
- Sponsor
- Zimmer Biomet
Total Shoulder Arthroplasty, Reverse Total Shoulder Arthroplasty
Continuous Interscalene Blocks and Rebound Pain
The primary objectives of this present study are to examine whether a continuous interscalene block of a total duration of 48 hours reduces the incidence of rebound pain comparatively to single-shot interscalene block, through…
- Conditions
- Total Shoulder Arthroplasty, Reverse Total Shoulder Arthroplasty, Interscalene Analgesia, Interscalene Blocks
- Trial name
- NCT07770165
- Testing
- Continuous interscalene nerve block, Interscalene Block
- Where
- Canada
- Volunteers
- 154 people
- Sponsor
- University of Calgary
Arthritis
S.E.S Shoulder Arthroplasty Data Collection
This observational study intends to collect efficacy and safety data on S.E.S shoulder system
- Trial name
- NCT00754416
- Where
- 12 sites in Belgium, France
- Volunteers
- 100 people
- Sponsor
- Zimmer Biomet
Rotator Cuff Tear Arthropathy, Massive Irreparable Rotator Cuff Tear
Impact of Glenosphere Size on Range of Motion in Female Patients Undergoing Reverse Shoulder Arthroplasty
The purpose of this study is to perform a prospective randomized trial among female patients undergoing reverse shoulder arthroplasty (RSA) to determine if a larger glenosphere allows greater range of motion without an impact on…
- Trial name
- NCT04093804
- Testing
- Glenosphere size for Reverse Shoulder Arthroplasty
- Where
- United States
- Volunteers
- 120 people
- Sponsor
- Fondren Orthopedic Group L.L.P.
Total Shoulder Arthroplasty
Patient Specific Instruments Versus Standard Surgical Instruments
Comparison of Glenoid Component Position Using Patient Specific Instruments Versus Standard Surgical Instruments: A Randomized Prospective Clinical Trial
- Trial name
- TIOSO-GPS (NCT01430468)
- Testing
- Glenoid Positioning System
- Where
- United States
- Volunteers
- 44 people
- Sponsor
- The Cleveland Clinic
Osteoarthritis of the Shoulder
Patients Experiences of Rehabilitation Before and After Reverse Shoulder Arthroplasty
Reverse shoulder arthroplasty is a complex surgical procedure requiring thorough rehabilitation, and its frequency is increasing globally.
- Trial name
- NCT06897124
- Where
- Sweden
- Volunteers
- 15 people
- Sponsor
- Vastra Gotaland Region
Pain, Shoulder
Continuous Interscalene Block for Same Day Discharge Following Total Shoulder Arthroplasty
Total shoulder surgeries are associated with considerable postoperative pain which may prevent rehabilitation and early discharge from the hospital.
- Trial name
- NCT01785940
- Testing
- Interscalene block
- Where
- Canada
- Volunteers
- 10 people
- Sponsor
- London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Osteoarthritis
Electromyography Evaluation of Subscapularis Function After Total Shoulder Arthroplasty
The primary objective is to document function of the structurally intact subscapularis after total shoulder arthroplasty by using electromyography. Structural integrity of the subscapularis will be confirmed using ultrasound.
- Trial name
- NCT00779974
- Testing
- Evaluation
- Where
- United States
- Volunteers
- 32 people
- Sponsor
- Milton S. Hershey Medical Center
Arthroplasty, Replacement, Shoulder
S-33 SMR Shoulder HP Reverse Glenosphere
Study Design: Single arm, retrospective and prospective, single center, post-market clinical study Purpose:To demonstrate the safety and effectiveness of the SMR Reverse HP Shoulder System device for primary, fracture or revision…
- Trial name
- NCT05339815
- Testing
- SMR shoulder arthroplasty
- Where
- United Kingdom
- Volunteers
- 205 people
- Sponsor
- Limacorporate S.p.a