Clinical trials: Fractures, Comminuted
Mandibular Fractures, Maxillofacial Injuries
Virtual Surgical Planning and Preoperative Plate Bending for Maxillofacial Fractures
Purpose: Complex mandibular fractures are commonly associated with high-energy maxillofacial trauma and may result in disruption of mandibular continuity, facial deformity, malocclusion, and impaired mastication and speech.
- Conditions
- Mandibular Fractures, Maxillofacial Injuries, Fractures, Comminuted
- Trial name
- NCT07856589
- Testing
- Conventional Open Reduction and Internal Fixation With Intraoperative Plate Bending, Virtual Surgical Planning-Assisted Open Reduction and Internal Fixation With Preoperative Plate Bending
- Where
- Vietnam
- Volunteers
- 30 people
- Sponsor
- University of Medicine and Pharmacy at Ho Chi Minh City
Proximal Interphalangeal Joint Fracture
Evaluation of Suzuki Frame Fixation in Comminuted Fractures of the Proximal Interphalangeal Joint.
This prospective randomized controlled trial aims to evaluate the functional and radiological outcomes of using the Suzuki frame for treating comminuted intra-articular fractures of the proximal interphalangeal (PIP) joint.
- Trial name
- NCT07714356
- Testing
- Suzuki Frame, Standard Conventional Treatment.
- Where
- Egypt
- Volunteers
- 2 people
- Sponsor
- Yehia Mohamed
Elbow Joint Destruction, Post-traumatic Lesions
Clinical Outcomes Study of the Nexel Total Elbow
The objectives of the study are to confirm safety and performance of the Zimmer Nexel Total Elbow when used in primary or revision total elbow replacement.
- Conditions
- Elbow Joint Destruction, Post-traumatic Lesions, Ankylosed Joints, Advanced Rheumatoid Arthritis
- Trial name
- NCT02469662
- Testing
- Nexel Total Elbow
- Where
- 11 sites in United States, Australia and 6 more
- Volunteers
- 134 people
- Sponsor
- Zimmer Biomet
Bone Fracture
Enhancement of Bone Regeneration and Healing in the Extremities by the Use of Autologous BonoFill-II
The purpose of this clinical study is to evaluate the safety and the efficacy of BonoFill-II as an autologous bone-regenerating graft in the reconstruction of deficient bone in two clinical indications: 1.
- Trial name
- NCT03024008
- Testing
- BonoFill-II
- Where
- 6 sites in Israel
- Volunteers
- 40 people
- Sponsor
- BonusBio Group Ltd
Fracture Tibia, Fracture Femur
3D Planned Surgery of Acute Fractures Performed With 3D Guides Printed at the Point of Care
The aim of the study is to assess the accuracy of fracture reduction performed with surgical guides designed and 3D printed at the point of care in comminuted fractures of femur- and tibia-shaft.
- Conditions
- Fracture Tibia, Fracture Femur, Fracture, Comminuted
- Trial name
- 3DFRG (NCT05741892)
- Testing
- Fracture reposition with 3D printed patient specific repositions guides
- Where
- Switzerland
- Volunteers
- 15 people
- Sponsor
- Insel Gruppe AG, University Hospital Bern
Distal Humerus Fracture, Comminuted Fracture
Elbow Hemiarthroplasty Versus ORIF for Distal Humeral Fractures
This is a randomized control trial comparing the outcome of ORIF (open reduction and internal fixation) with EHA (elbow hemiarthroplasty) for distal humeral fractures in patients aged 50 years or above.
- Conditions
- Distal Humerus Fracture, Comminuted Fracture, Intra-Articular Fractures
- Trial name
- NCT04163172
- Testing
- Surgical treatment of distal humeral fracture with elbow hemiarthroplasty, Surgical treatment of distal humeral fracture with double plating.
- Where
- Denmark
- Volunteers
- 44 people
- Sponsor
- Herlev and Gentofte Hospital
Fracture, Closed, Comminuted, Healing
Electromagnetic Stimulation as Coadjuvant in the Healing of Diaphyseal Femoral Fractures
This study specifically evaluates the effects of electromagnetic stimulation for diaphyseal femur fractures using a device developed by the investigators.
- Trial name
- NCT02188836
- Testing
- Electromagnetic stimulation
- Where
- Colombia
- Volunteers
- 64 people
- Sponsor
- Fundacion Clinica Valle del Lili
Closed Non Comminuted Long Bone Fractures
Continuous Lornoxicam Infusion for Orthopaedic Surgery
Perioperative continuous infusion of lornoxicam would be an effective and safe regimen to reduce the patient controlled morphine consumption after orthopaedic surgery.
- Trial name
- NCT01718756
- Testing
- Continuous infusion, Scheduled
- Where
- Egypt
- Volunteers
- 96 people
- Sponsor
- Mansoura University
Comminuted Fracture Tibia
Comminuted Fractures of the Midshaft of the Tibia; (Interlocking Nail +/- Blocking Screws or Locked Plating With Predicted Distribution of Locking Screws) Choice Based on Finite Element Analysis Correlated With Clinical Outcome and Union.
study is to assess the clinical and radiological results of Comminuted fractures of the midshaft of the tibia; treated with interlocking nail +/- blocking screws or locked plating with predicted distribution of locking screws…
- Trial name
- Finite Element (NCT04388462)
- Testing
- Finite element analysis
- Where
- Egypt
- Volunteers
- 20 people
- Sponsor
- Cairo University
Fractures, Comminuted, Surgical Wound Dehiscence
Application of Indocyanine Green Angiography for Closed Operative Calcaneus Fractures
Researchers in the Orthopaedic surgery department at LSU Medical Center-Shreveport hope to learn if patterns of blood-flow around the incision site of patients undergoing surgery for heel-bone fractures can help predict whether…
- Conditions
- Fractures, Comminuted, Surgical Wound Dehiscence, Necrosis
- Trial name
- NCT01693484
- Testing
- ICG (Indocyanine Green)
- Where
- United States
- Volunteers
- 13 people
- Sponsor
- Louisiana State University Health Sciences Center Shreveport
Upper Extremity Fracture, Upper Extremity Dislocation
Progressive Splinting Status Post Elbow Fractures and Dislocations
The purpose of this study is to help determine if a static stretching brace in addition to physical therapy decreases the incidence of secondary operations, increases range of motion, and individual patient function.
- Conditions
- Upper Extremity Fracture, Upper Extremity Dislocation, Fractures, Comminuted, Elbow Fracture
- Trial name
- JAS (NCT00580866)
- Testing
- JAS Brace
- Where
- United States
- Volunteers
- 17 people
- Sponsor
- Vanderbilt University
Fracture, Closed, Comminuted, Healing
Effect of Low-Magnitude, High Frequency Vibration Treatment on Femoral Shaft Fracture Healing
Diaphyseal long bone fractures are usually associated with high energy trauma in which femoral shaft fracture is one common fracture in young age group.
- Trial name
- NCT01386749
- Testing
- vibration platform provide low magnitude and high frequency vibration treatment, which is self-developed by our research team
- Where
- China
- Volunteers
- 50 people
- Sponsor
- Chinese University of Hong Kong
Fractures, Comminuted, Fracture Fixation, Internal
Comparative Study of Fixation or Fusion of Calcaneal Fractures
A multicentre randomized controlled trial that will be conducted at Level 1 trauma centres across Canada. It will compare patients who receive open reduction, internal fixation for Sanders IV calcaneal fractures to patients who…
- Trial name
- Sanders IV (NCT00679393)
- Testing
- Open reduction internal fixation, Fusion
- Where
- 4 sites in Canada
- Volunteers
- 26 people
- Sponsor
- University of Calgary
Fracture, Closed, Comminuted, Healing
Treatment of Displaced Lateral Clavicle Fractures Using a Locking Compression Plate With Lateral Extension
Treatment of lateral fractures of the clavicle is challenging and has been controversially discussed for a long time due to high non-union rates in non-operative treatment and high complication rates in surgical treatment.
- Trial name
- LatClav (NCT02256059)
- Testing
- Plate osteosynthesis
- Where
- Germany
- Volunteers
- 20 people
- Sponsor
- Technical University of Munich
Closed Comminuted Oblique Intertrochanteric Fracture of Neck of Right Femur, Closed Comminuted Oblique Intertrochanteric Fracture of Neck of Left Femur
Comparing Weight Bearing After Intramedullary Fixation Devices for the Proximal Femur Fracture
The purpose of the study is to Compare the stability of the fracture and pain after surgery by measuring the stride length and weight bearing on the operated leg.
- Trial name
- NCT01509859
- Testing
- PFNA proximal femur nail device (Synthes), INTERTAN proximal femur nail device (Smith&Nephew)
- Where
- Israel
- Volunteers
- 100 people
- Sponsor
- Rabin Medical Center