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Ankle Fractures clinical trials

View clinical trials related to Ankle Fractures.

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NCT ID: NCT01742650 Completed - Trauma Clinical Trials

Screw Versus Tightrope Syndesmotic Injury Fixation in Weber C Ankle Fractures

Start date: July 2010
Phase: N/A
Study type: Interventional

The aim of our study is to compare two different syndesmosis transfixation methods in AO/OTA Weber C ankle fractures. Our hypothesis is that 50% of screw fixed fibulas but only 5% of suture-button fixed fibulas are in malposition. All skeletally mature patients (16 years or older) with AO/OTA Weber C type fractures operated within a week after trauma are consecutively included into the study. The tibiofibular transfixation is randomly performed either by a 3,5 mm tricortical screw or a suture-button (TightRope). Malposition of the tibiofibular joint is assessed in an intraoperative computed tomography. Clinical outcome is assessed by using Olerud-Molander, RAND ja 36-Item Healt Survey after 1-year from the injury.

NCT ID: NCT01729195 Completed - Ankle Fracture Clinical Trials

Ankle Syndesmosis Fixation by Antibiotic Releasing Bioabsorbable Screw

Start date: March 2006
Phase: Phase 2
Study type: Interventional

This single-center randomized trial evaluates the efficacy and safety of a new bone screw (antibiotic releasing bioabsorbable screw) in fixation of syndesmosis in patients with Weber C-type ankle fractures. The comparison is made to subjects treated by conventional metal screw fixation of the syndesmosis. The primary objective is to show that the antibiotic releasing bioabsorbable screw is at least as good as the routinely used metal screw in prevention of syndesmosis widening in patients with Weber C-type ankle fractures. The secondary objective is to show that the clinical outcome of the ankle fracture treatment is equal between patients treated by the antibiotic releasing bioabsorbable screw and the conventional metal screw.

NCT ID: NCT01616173 Completed - Fracture of Ankle Clinical Trials

Analgesic Benefits of Perineural Versus Intravenous Dexamethasone in Patients Receiving Sciatic Nerve Block

Start date: June 2012
Phase: Phase 4
Study type: Interventional

Patients scheduled to have foot and ankle surgery will typically receive a single shot sciatic nerve block to serve as the primary anesthetic and as part of a multi-modal post-operative analgesic plan. The investigators are investigating the use of perineural dexamethasone together with local anesthetics can improve the quality of recovery for patients receiving sciatic nerve blocks for foot and ankle surgery.

NCT ID: NCT01561365 Completed - Ankle Sprain Clinical Trials

Applicability of the Ottawa Ankle Rules

Start date: October 2003
Phase: N/A
Study type: Interventional

The aim of this prospective study was to compare outcomes in patients handled by emergency physician according to OAR versus by an orthopedic resident. 92 consecutive patients with ankle injuries attending our emergency department were divided in two groups. The study group comprised 32 patients who arrived during the morning shift and were examined by an emergency physician according to OAR. Patients discharged without an x-ray were followed in the clinic or by telephone communication. The control group constituted 60 patients who were examined during the evening and night shifts by orthopedic residents unaware of this study.

NCT ID: NCT01493167 Completed - Bone Fracture Clinical Trials

Study on Wood-plastic Composite for Circumferential Casting

WOODCAST
Start date: December 2011
Phase: N/A
Study type: Observational

The purpose of study is to verify that WOODCAST Circular system performs safely and effectively in its intended use.

NCT ID: NCT01484535 Completed - Ankle Fracture Clinical Trials

Aspiration for Pain Relief Following Ankle Fracture

Start date: September 2011
Phase: N/A
Study type: Interventional

This trial will study the effect of hematoma aspiration in patients with acute ankle fractures.

NCT ID: NCT01444144 Completed - Ankle Fracture Clinical Trials

Ankle Fracture Treatment in the Elderly

Start date: March 2011
Phase: N/A
Study type: Observational

The purpose of this study is to track surgical outcomes and post-operative course in patients 55 years of age or older treated for ankle fractures.

NCT ID: NCT01441817 Completed - Fracture of Ankle Clinical Trials

Non--operative Treatment of the Medial Malleolus in bi- and Trimalleolar Ankle Fractures

Start date: May 2002
Phase: N/A
Study type: Interventional

The purpose of this study was to determine if internal fixation of the medial malleolus is necessary following open reduction and internal fixation of the lateral and, if required, the posterior malleolus treating displaced bi-or trimalleolar ankle fractures.

NCT ID: NCT01431560 Completed - Ankle Fracture Clinical Trials

Outcomes of Operative Treatment of Unstable Ankle Fracture - Comparison Between Metallic and Biodegradable Implants

Start date: June 2008
Phase: Phase 4
Study type: Interventional

The purposes of this study are to compare the outcomes of the biodegradable implants for the fixation of ankle fracture and those of metallic implants, and to assess the problems of the biodegradable implants. Null hypothesis is that the clinical outcomes of biodegradable plate and screws for ankle fracture are not different from those of metallic implants.

NCT ID: NCT01341015 Completed - Ankle Fracture Clinical Trials

Bedside Ultrasound in the Diagnosis of Ankle Fractures in Children

Start date: June 2010
Phase: Phase 0
Study type: Interventional

Objectives: A lot of children who injure their ankles come to the emergency department for an evaluation, and often an X-ray of the ankle is obtained to determine if a bone fracture is present. In more than 85% of cases, however, the injury is a sprain and not a bone fracture and can be treated with rest, ice, elevation, and pain medications. X-rays obtained in the emergency departments are time consuming, often uncomfortable for the patient, and expose children to radiation, the long-term effects of which are not yet fully understand by doctors or scientists. Bedside ultrasound is a non-invasive and a non-painful device that does not produce radiation. It was been shown to determine the presence of bone fracture in childrens' wrists and forearms just as well as X-rays do. In our study, the investigators would like to determine if a bedside ultrasound can also be used to evaluate ankle fractures in children. Research Procedures: In our study, the investigators will ask the parents and children, who are scheduled to get an X-ray of their ankle in the emergency department, to examine their ankles with an ultrasound machine as well. Since the bedside ultrasound is not significantly time-consuming, does not require patients to remain still, and is readily available in the department, the procedure will be performed while kids are waiting to get an X-ray, getting registered, or awaiting further treatment. On the data collection form, the investigators will document the patients' names, birthdates, medical record numbers so that their X-ray results can be compared to the ultrasound results for the purpose of the study. The information will be stored in a secure cabinet in a locked office. The investigators will also document which side is injured, where the patient feels pain and what the ankle looks like to help perform the ultrasound. The results of both the ultrasound and X-ray will be documented for each patient.