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Tibial Fracture clinical trials

View clinical trials related to Tibial Fracture.

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NCT ID: NCT05012449 Active, not recruiting - Tibial Fracture Clinical Trials

Transitional Ankle Fracture Management Using a New Joystick Technique

Transitional
Start date: July 1, 2021
Phase: N/A
Study type: Interventional

To investigate the feasibility and short-term clinical efficacy of the arthrography-assisted joystick technique for the treatment of adolescent transitional ankle fracture.

NCT ID: NCT04432389 Recruiting - Tibial Fracture Clinical Trials

Study to Assess the Efficacy and Safety of Allogeneic Osteoblastic Cells (ALLOB®) Single Implantation in Tibial Fracture

ALLOB-TF2
Start date: January 8, 2021
Phase: Phase 2
Study type: Interventional

Although the majority of tibial fractures heal normally, some fractures may not heal within the usual time frame and is known as delayed bone healing within 4 to 6 months and absence of bone healing within 9 to 12 months in the most severe case of. Several factors can increase the risks of delayed healing complications like, for example, smoking, violent shocks (for example, due to a road accident) or even the type of fracture (an open fracture). The location of the fracture is also an important factor: among the bones of the arms and legs, the tibia is known for being the most at risk for complications. At tibial fracture with several risk factors could lead to delayed complications and interfere with patient daily life and reduce the quality of life. The study drug, ALLOB®, is constituted of bone cells produced from the bone marrow of healthy adult donors. Preclinical studies have shown that ALLOB® cells are capable of forming bone and repairing fractures. When directly injected into a fracture, ALLOB® should therefore promote the healing of the fracture by re-establishing a healthy environment and stimulating bone production. To date, there is no treatment for fractures considered at risk of delayed complications. The current practice on diagnosis of complications is to wait at least 6-12 months before considering alternative interventions to promote fracture healing. The injection of ALLOB® quickly after the fracture should stimulate bone healing, reduce healing time, reduce complications, and improve the quality of life for the patient. ALLOB® has already shown preliminary evidence of effectiveness in the treatment of delayed bone healing fractures (ALLOB-DU1 clinical trial), including tibial fractures (8 patients). With this study, the Sponsor will evaluate whether ALLOB® promotes the healing of tibial fractures compared with placebo.

NCT ID: NCT04028908 Completed - Tibial Fracture Clinical Trials

Remodelling After Trampoline Fracture in Children

Start date: February 10, 2016
Phase:
Study type: Observational

The anterior tilting of the proximal tibia epiphyseal plate is a radiological tool for the diagnosis of suspected trampoline fracture. The tibial fracture leads to a ventral tilting of the tibial Plateau. This study is to document the long-term follow-up of the anterior tilt angle and to verify, if there is an uplift of the tibia plateau with correction of the anterior tilt angle to normal values (= remodelling) in order to guarantee optimal treatment of this rare fracture.

NCT ID: NCT03598530 Active, not recruiting - Tibial Fracture Clinical Trials

Fracture-Related Outcome Study for Operatively Treated Tibia Shaft Fractures

FROST
Start date: April 4, 2019
Phase:
Study type: Observational [Patient Registry]

Approximately 1000 patients presenting with tibial shaft fractures (AO type 42) will be enrolled prospectively in this registry. All patients are treated and followed at 6 weeks, 6 months and 1 year postoperative always following the local standard of care (routine) visit schedule up to 36 months if required. Data collection includes patient and fracture details, treatment details, functional, clinical and patient-reported outcomes and anticipated or procedure- and implant-related adverse events (i.e. complications) and their corresponding treatment

NCT ID: NCT02820363 Completed - Tibial Fracture Clinical Trials

Study Evaluating CERAMENTâ„¢|G in Open Diaphyseal Tibial Fractures

Start date: February 14, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to demonstrate the safety and effectiveness of CERAMENTâ„¢|G used in conjunction with standard-of-care treatment compared to standard-of-care treatment alone in the care of subjects with open fractures of the tibial diaphysis.

NCT ID: NCT02140528 Completed - Tibial Fracture Clinical Trials

Allogeneic Mesenchymal Stem Cell Transplantation in Tibial Closed Diaphyseal Fractures

Start date: August 2013
Phase: Phase 2
Study type: Interventional

This study is a case-control prospective, clinal trial to assess the safety and efficacy of the allogeneic adipose derived mesenchymal stem cell transplantation on the healing of recent tibial fracture in 40 patients.

NCT ID: NCT02035917 Unknown status - Tibial Fracture Clinical Trials

Comparison of Tibial Plateau Fractures Outcomes Treated With Non-locking and Locking Plate

Start date: n/a
Phase: N/A
Study type: Interventional

this study will perform to compare the results and functional outcomes of tibial plateau fractures treated with non-locking and locking plate fixation.

NCT ID: NCT01955577 Not yet recruiting - Tibial Fracture Clinical Trials

Vitamin D Supplement for Patients With Tibial Fracture

Start date: April 2015
Phase: Phase 1
Study type: Interventional

The purpose is to study: 1. the frequency of vitamin D deficiency at patients with tibial fracture treated with an external ring fixator 2. if vitamin D supplement facilitates fracture healing 3. a possible relation between vitamin D deficiency and the risk of complications and the time of fracture healing

NCT ID: NCT01927575 Terminated - Tibial Fracture Clinical Trials

Pilot Study Comparing Diagnostic Imaging Versus Tomosynthesis in Detection of Hip, Wrist or Tibia Injury

TOMO
Start date: September 2013
Phase: N/A
Study type: Interventional

To acquire and build a library of image sets to determine if Fuji's TOMO imaging device can replace or compliment current imaging standards to assess patients with hip, wrist or tibia injuries.

NCT ID: NCT01795287 Recruiting - Tibial Fracture Clinical Trials

Safety of Spinal Anesthesia in Patients With Tibial Shaft Fracture

Start date: March 2012
Phase: N/A
Study type: Interventional

There is a elevated risk of acute compartment syndrome (ACS) related to tibial shaft fractures due to oedema and reduced blood flow in traumatised tissues. This may lead to lack of oxygen and even necrosis. Symptoms of ACS are severe pain, hypoaesthesia, pain during flexion of the ankle and swollen leg in clinical examination. Paralysis and lack of distal pulses are late symptoms of ACS. Many experts think that effective relief of pain caused by regional anaesthesia (RA) may hide the symptoms of the ACS. This may be incorrect. The evidence of dangers related to RA is based on old patient-series and single case-reports. Some of these studies report the symptoms of ACS (hypaesthesia and even pain) being caused by RA. Majority of the conclusions in these studies cannot be confirmed by an expert of RA. It is also possible that there are more hemodynamic changes related to general anaesthesia (GA) which may predispose to ACS. There are no modern, randomized and controlled studies of the safety of RA in patients with tibial shaft fracture.