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Ankle Fractures clinical trials

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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.

NCT ID: NCT01338129 Not yet recruiting - Ankle Fracture Clinical Trials

The Effect of Vitamin c on Preventing Complex Regional Pain Syndrome (CRPS Type I) Following Ankle Fracture

CRPS
Start date: April 2011
Phase: N/A
Study type: Interventional

The use of prophylactic treatment with vitamin c may prevent complex regional pain syndrome (CRPS)

NCT ID: NCT01234493 Completed - Trauma Clinical Trials

Syndesmotic Injury and Fixation in Supination-External (SE) Ankle Fractures

Start date: June 2007
Phase: N/A
Study type: Interventional

The aim of our study was to determine whether transfixation of unstable syndesmosis is necessary in supination-external rotation type ankle fractures. Our hypothesis was that syndesmotic ligaments heal at the proper length after malleolar reduction and that syndesmotic transfixation is not needed in supination-external rotation fracture types.

NCT ID: NCT01196338 Recruiting - Ankle Injuries Clinical Trials

Early Weightbearing and Mobilization Versus Non-Weightbearing and Mobilization in Unstable Ankle Fractures

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

The primary objective of the investigators randomized controlled trial is to determine if early protected weightbearing and ankle range of motion after surgical treatment (open reduction internal fixation - ORIF) for ankle fractures improves the rate of return to work and functional outcome compared to postoperative ankle immobilization in a non-weightbearing cast.

NCT ID: NCT01134354 Completed - Clinical trials for Tibia Fracture (Isolated)

The Role of Patient Expectations in Traumatic Orthopedic Outcomes-TEFTOM EURASIA

Start date: June 2010
Phase: N/A
Study type: Observational

Design: Prediction trial, up to 10 sites in Asia and Europe Goal: To better understand the "success" or "failure" after orthopedic trauma surgery by developing a model that can be applied clinically as a user-friendly "baseline" questionnaire - capable of predicting "success" or "failure" based on a patient's pre-surgical expectations of their final outcome and to validate a novel outcomes measure (TOM). Primary aim: To assess the psychometric properties of predictive validity, internal consistency and reproducibility of the trauma expectation factor (TEF) in the Eurasian population. Secondary aim: To assess the psychometric properties of criterion validity, internal consistency,reproducibility, and sensitivity to change of the TOM in the Eurasian population. Key questions related to patient and surgeon expectations: - How different, or similar, are patient and surgeon expectations? - Do expectations change over time? - Do patient expectations predict outcomes in validated measures use today?

NCT ID: NCT01134094 Completed - Ankle Fractures Clinical Trials

Combined Randomised and Observational Study of Type B Ankle Fracture Treatment

CROSSBAT
Start date: August 2010
Phase: N/A
Study type: Interventional

This study will determine whether operative management confers improved short and long−term outcomes for patients with isolated AO type 44−B1 distal fibula fractures when compared with non−operative management.