Clinical trials: Humerus
Distal Humerus Fracture
Hemiarthroplasty Or Total Elbow Arthroplasty in the Elderly.
A feasibility study to assess the practicality, and obtain preliminary data to inform, a definitive Randomise Control Trial (RCT) in patients over the age of 65 diagnosed with un-reconstructible distal humeral fractures, to…
- Trial name
- HOT (NCT04646798)
- Testing
- Hemiarthroplasty, Total elbow arthroplasty
- Where
- 2 sites in United Kingdom
- Volunteers
- 20 people, healthy volunteers welcome
- Sponsor
- Royal Devon and Exeter NHS Foundation Trust
Lateral Condyle Fractures,Humerus,JakobⅡ Classification,Reduction
Surgical Treatment for the Displaced JakobⅡ Classification Humerus Lateral Condylar Fractures in Children
Multi-center Study on Surgical Treatment for the Displaced JakobⅡ Classification Humerus Lateral Condylar Fractures in Children.
- Trial name
- JCHLCF (NCT03447496)
- Testing
- Closed reduction, Open reduction
- Where
- China
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Shunyou Chen
Distal Humerus Fracture, Distal Femur Fracture
3D-printed Bone Models in Addition to CT Imaging for Intra-articular Fracture Repair
The purpose of this study is to compare the effectiveness of 3D-printed bone models in addition to CT imaging versus CT imaging alone on surgical quality and operation time for patients undergoing surgical repair of…
- Conditions
- Distal Humerus Fracture, Distal Femur Fracture, Distal Tibia Fracture, Proximal Humeral Fracture
- Trial name
- SPRINT (NCT04748016)
- Testing
- 3D printed (3DP) bone models + CT imaging, CT imaging
- Where
- Hong Kong
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- The University of Hong Kong
Osteoarthritis Shoulder, Avascular Necrosis of the Head of Humerus
Catalyst CSR Shoulder System for Semi or Total Shoulder Arthroplasty
Evaluation of the performance and safety of the Catalyst CSR Shoulder System with clinical and radiographic results at multiple time points through 24 months postoperatively This study will be a prospective multi-center study…
- Conditions
- Osteoarthritis Shoulder, Avascular Necrosis of the Head of Humerus, Rheumatoid Arthritis Shoulder
- Trial name
- NCT04968405
- Testing
- Catalyst CSR Total Shoulder System
- Where
- 3 sites in United States
- Volunteers
- 87 people, healthy volunteers welcome
- Sponsor
- Catalyst OrthoScience
Vascular Access
Evaluation of Various Methods Used to Identify the Proximal Humerus Intraosseous Vascular Access Site
The purpose of this study is to determine if there is one method of identifying the proximal humerus intraosseous vascular access site that is easier for clinicians to use, out of the 4 methods being evaluated.
- Trial name
- NCT01742780
- Testing
- Intraosseous Vascular Access
- Where
- United States
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Vidacare Corporation
Rotator Cuff
The Research About the Function of the Rotator Cuff After Humeral Greater Tuberosity Fractures
The purpose of this retrospective study was to investigate the differences in fracture block and rotator cuff function in patients with rotator cuff injuries due to greater tuberosity humerus fractures.
- Trial name
- NCT07368725
- Testing
- without intervention
- Where
- China
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Guo Jialiang
Elbow Fracture
Radiation Therapy for Heterotopic Ossification Prophylaxis Acutely After Elbow Trauma
The investigators hypothesized that radiation therapy could be safely administered acutely after elbow trauma, and it would decrease the number of patients that would require surgical excision of heterotopic ossification.
- Trial name
- ElbowHO (NCT00991887)
- Testing
- Radiation Therapy (XRT)
- Volunteers
- 48 people, healthy volunteers welcome
- Sponsor
- Wake Forest University Health Sciences
Humeral Fractures
Treatment of Proximal Humerus Fractures in the Elderly
This study is set to evaluate a proposed standard for the treatment of proximal humerus fractures
- Trial name
- prox_hum (NCT02566018)
- Testing
- treatment/medical device, standard
- Where
- Switzerland
- Volunteers
- 160 people, healthy volunteers welcome
- Sponsor
- University Hospital, Basel, Switzerland
Supracondylar Fracture, Morbidity
Comparison of Day-time and Night-time Operations of Supracondylar Humeral Fractures
This study aims to investigate that performing supracondylar humerus fracture operations during daylight hours may have better results than performing them at night.
- Trial name
- NCT04694469
- Testing
- Closed reduction and percutaneous pinning (CRPP)
- Where
- Turkey (Türkiye)
- Volunteers
- 82 people, healthy volunteers welcome
- Sponsor
- Istanbul University
Osteo Arthritis Shoulders, Avascular Necrosis of the Head of Humerus
Easytech Reversed Shoulder System Clinical Study
The purpose of the study is to collect data to demonstrate the safety and effectiveness of the Easytech Reversed Shoulder System for the treatment of patients who require a reverse total shoulder arthroplasty.
- Conditions
- Osteo Arthritis Shoulders, Avascular Necrosis of the Head of Humerus, Rotator Cuff Tear
- Trial name
- NCT03806842
- Testing
- Easytech group
- Where
- 6 sites in United States
- Volunteers
- 90 people, healthy volunteers welcome
- Sponsor
- FX Shoulder Solutions
Proximal Humerus Fracture (Shoulder Fracture)
Shoulder Fracture Interview Study
Shoulder fractures are painful injuries and are the third most common fracture in adults. More and more people are having these injuries each year.
- Trial name
- NCT05905471
- Testing
- Interview
- Where
- United Kingdom
- Volunteers
- 14 people, healthy volunteers welcome
- Sponsor
- East Lancashire Hospitals NHS Trust
Transhumeral Amputation
EFS Functional Expectations of Transhumeral Percutaneous OI Patients
An FDA Early Feasibility Study (EFS) allows for early clinical evaluation of devices to provide proof of principle and initial clinical safety data.
- Trial name
- AEA PODS (NCT03824444)
- Testing
- PODS
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- VA Office of Research and Development
Proximal Humeral Fracture
Proximal Humerus Fractures: A Retrospective Analysis
The purpose of this study is to evaluate preoperative objective measurements of patients with a proximal humerus fracture and operative objective measurements to determine if there is any effect to postoperative outcomes.
- Trial name
- PHFx (NCT03637608)
- Where
- United States
- Volunteers
- 94 people, healthy volunteers welcome
- Sponsor
- The Orthopaedic Research & Innovation Foundation
Intraosseous Vascular Access, Vascular Access
Follow-Up Study Validating a Blended Technique to Identify the Proximal Humerus Intraosseous Vascular Access Site
A Follow-up Study Validating a Blended Technique for Identifying the Proximal Humerus Intraosseous Vascular Access Insertion Site
- Trial name
- NCT01866501
- Testing
- Intraosseous Vascular Access
- Where
- United States
- Volunteers
- 15 people, healthy volunteers welcome
- Sponsor
- Vidacare Corporation
Intraosseous Access, Resuscitation
Trial Comparing Proximal Tibia and Proximal Humerus Infusion Rates Using the NIO Intraosseous Device
The investigators sought to compare the intraosseous access success rates of the proximal tibia and the proximal humerus using new Intraosseous access device "NIO" in an adult cadaver model during simulated resuscitation.
- Trial name
- IOACS (NCT02700867)
- Testing
- NIO
- Where
- Poland
- Volunteers
- 84 people, healthy volunteers welcome
- Sponsor
- Medical University of Warsaw
Reverse Total Shoulder Arthroplasty
Reverse Total Shoulder Arthroplasty in Patients Who Exceeded Their Life-expectancy: a Retrospective Study
Reverse total shoulder arthroplasty (RTSA) has become an established treatment for cuff arthropathy, severe osteoarthritis and in certain fracture cases.
- Trial name
- NCT04807322
- Testing
- Reverse Total Shoulder Arthroplasty (RTSA)
- Where
- Switzerland
- Volunteers
- 110 people, healthy volunteers welcome
- Sponsor
- Bürgerspital Solothurn
Distal Humerus Fracture
Retrospective Analysis on Distal Humerus Fractures
The purpose of this study is to evaluate preoperative objective measurements for distal humerus ORIF patients and operative objective measurements to determine if there is any effect to postoperative outcomes.
- Trial name
- (DHFx) (NCT03637621)
- Testing
- ORIF
- Where
- United States
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- The Orthopaedic Research & Innovation Foundation
Elbow Fracture, Elbow Arthropathy
Can Secondary Total Elbow Arthroplasty After Failed Internal Fixation or Non-operative Treatment of Distal Humeral Fractures Achieve Equal Results as Primary Arthroplasty?
Total elbow arthroplasty (TEA) results in immediate pain release with good functional results after distal humerus fractures. But still open reduction and internal fixation is recommended as treatment of choise due to a lifelong…
- Trial name
- NCT03302533
- Testing
- Total elbow arthroplasty
- Volunteers
- 23 people, healthy volunteers welcome
- Sponsor
- Diakoniekrankenhaus Friederikenstift