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Tibial Fractures clinical trials

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NCT ID: NCT03314623 Completed - Clinical trials for Surgery--Complications

Immediate Mobilization After Plate Osteosynthesis of Proximal Tibial Fractures - A Cohort Study

IMOP
Start date: February 1, 2018
Phase:
Study type: Observational

The purpose of this study is to investigate if immediate mobilization with weight bearing as tolerated following surgery with plates and screws after a fracture of the shinbone near the knee is possible without increased risk. The investigators hypothesize immediate weight bearing as tolerated following surgery with plates and screws of the above mentioned fracture, in cases deemed stable by the surgeon, will not lead to any loss of reduction.

NCT ID: NCT03232216 Recruiting - Clinical trials for Vitamin D Deficiency

Vitamin D Supplementation and Tibia Fracture. Does it Improve Healing Rate?

ViDco
Start date: November 21, 2017
Phase: N/A
Study type: Interventional

This study evaluates the effect of Vitamin D3 supplementation in healing rate of tibia fractures in adult patients with low vitamin D. Half of participants will receive Vitamin D3 supplementation while the other will receive placebo.

NCT ID: NCT03172715 Recruiting - Tibial Fractures Clinical Trials

Prosthesis Versus Osteosynthesis in Proximal Tibia Fractures

POSITIF
Start date: January 9, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to compare knee function and pain one year after treatment of intra-articular proximal tibia fracture using either osteosynthesis with a locking plate (ORIF) or primary total knee replacement (TKR) in patients over 65 years of age.

NCT ID: NCT03166267 Completed - Tibial Fractures Clinical Trials

Real Life Weight Bearing After Tibial Fractures

Start date: May 24, 2018
Phase:
Study type: Observational

In this prospective case series patients with a tibial fracture are monitored with smart biofeedback systems to document the healing progression and real life weight.

NCT ID: NCT03148067 Completed - Clinical trials for Surgical Wound Infection

Incidence and Risk Factors for Surgical Site Infection After Intramedullary Nailing of Femoral and Tibial Fractures

Start date: September 15, 2015
Phase:
Study type: Observational

Diaphyseal femoral and tibial fractures are in the spotlight within the traumatology-orthopedics scenario. Intramedullary nailing (IMN) remains the method of choice for treating these fractures, both open and closed ones. Occurrences of surgical site infection (SSI) related to this type of osteosynthesis are a challenge for all the professionals involved in patient healthcare. The reported incidence of SSI after IMN ranges from 0.9 to 17.5%. The majority of the data comes from retrospective studies and as part of case series descriptions, with little detail about the criteria used for defining and searching for cases of infection. Regarding the potential risk factors for this complication, previous use of external fixators, occurrence of open fractures and the severity of exposure according to the Gustilo-Anderson classification were indicated in a few retrospective studies as being possibly related to this complication. The objectives of the present observational cohort study are: 1. To determine the incidence of SSI related to IMN for fixation of diaphyseal femoral and tibial fractures in patients treated in a university traumatology and orthopedics reference hospital in São Paulo, Brazil; 2. To evaluate the risk factors related to the occurrence of this type of infection.

NCT ID: NCT03059368 Completed - Tibial Fractures Clinical Trials

New Bone Fixation Plate for the Repair of Tibial Avulsion Fracture of Posterior Cruciate Ligament of the Knee

Start date: August 2013
Phase: N/A
Study type: Interventional

To construct a self-designed plate fixation device for posterior cruciate ligament reconstruction, aim to verify its advantages on anatomical knee stability, so as to achieve fracture healing and keep tension after posterior cruciate ligament reconstruction.

NCT ID: NCT03042546 Terminated - Clinical trials for Open tíbia Fracture With Sub-segmental Bone Loss

Calcium Sulfate Spacer in Open Tibia Fractures

Start date: February 1, 2017
Phase: Phase 4
Study type: Interventional

Investigators will compare antibiotic impregnated Calcium sulfate versus PMMA versus nothing in these sub-segmental bone defects.

NCT ID: NCT03042533 Terminated - Clinical trials for Closed Transverse Fracture of Shaft of Tibia

Union Rate of Transverse Tibia Fracture

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

The investigators will compare the three methods of seating a tibial nail - Backslapping or Backslapping with Dynamic Locking or Internal Compression.

NCT ID: NCT02951884 Terminated - Tibial Fractures Clinical Trials

Intra-articular Local Anesthetic Injection and Hematoma Aspiration

Start date: June 15, 2016
Phase: Phase 4
Study type: Interventional

The primary objective of this study is to determine whether a patient with a tibial plateau fracture (non-displaced, displaced, or depression type) will have decreased pain and narcotic analgesia requirements following an intra-articular injection of local anesthetic and aspiration of the knee.

NCT ID: NCT02845245 Terminated - Tibial Fractures Clinical Trials

Comminuted Intra-Articular Distal Tibia Fracture Fixation Using Computer Techniques

CIDUCT
Start date: September 2016
Phase: N/A
Study type: Interventional

Comminuted intra-articular distal tibia fractures (OTA 43-C) typically are the result of high-energy trauma such as motor vehicle collisions or fall from a height. They are complex injuries often associated with significant fragment displacement and severe soft tissue injury, a combination that has long challenged orthopedic surgeons. Traditionally, surgeons use plain film (X-ray) and CT scans (2 or 3 dimensional) to determine fracture pattern and displacement. Yet, in some cases, it is still difficult to identify the relationship among bone fragments, which often makes articular restoration challenging. As a result, patients with non-anatomic joint reconstructions have a higher rate of poor outcomes. The primary objective of this study will be to compare patient outcomes in two groups, one group who will receive enhanced pre-operative planning (3D printed plastic prototype + standard of care [SOC] imaging with 3D CT scan + plain film radiographs) and a second group who will receive pre-operative planning using SOC imaging alone (3D CT scan + plain film radiographs only). Patient outcomes collected throughout the 12 month post-operative period will include an assessment of radiographic fracture healing (union, non-union, malunion), pain using a Numeric Pain Rating Scale, Olerud and Molander Score based on patient's self-report, and development of complications (infection, wound healing, re-operation, and re-hospitalizations). The secondary objective of this study will be to evaluate whether utilizing an enhanced pre-operative plan with a 3D printed plastic prototype altered the original pre-operative plan based on SOC imaging alone (3D CT scan + plain film radiographs only).