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Fracture clinical trials

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NCT ID: NCT03067454 Completed - Fracture Clinical Trials

Early Mobilization of Spiral Metacarpal Fractures Compared With Operative Treatment

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

Spiral metacarpal fractures (metacarpal II-V) can be treated conservatively or with operation. With minimal displacement this fracture is usually treated with immobilisation or early mobilisation. With appreciable displacement especially any malrotation the patient usually is treated with an operation. This usually includes an open reduction of the fracture and fixation with plates and screws or just screws. Even if this is an standard procedure both mild and severe complications have been reported. New studies have shown that even displaced fractures can be treated with early mobilization. In those cases the fractures may heal with some shortening but very good function. An advantage of early mobilization is that the patient avoids the risk of an operation and the costs for the treatment are decreased markedly. The study is designed to answer the question if early mobilization is not inferior to operative treatment but with lower costs and without any operation related risks.

NCT ID: NCT02933359 Completed - Fracture Clinical Trials

Osteogenic Profiling of Normal Calvarial Bone

Start date: October 2010
Phase:
Study type: Observational

The primary objectives of this study are: i) to procure human calvarial bone, ii) to grow cells from these tissues in vitro, iii) and to evaluate the osteogenic potential of these cells.

NCT ID: NCT02823925 Completed - Pain Clinical Trials

Bisphosphonate Therapy in MONA Spectrum Disorder

Start date: February 2013
Phase: N/A
Study type: Observational

Multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder is a rare inherited progressive skeletal disorder caused by mutations in the matrix metalloproteinase 2 (MMP2) gene. Treatment options are limited. The investigators reviewed the outcome of patients affected with MONA and treated with intravenous bisphosphonates in the clinical Center.

NCT ID: NCT02815423 Not yet recruiting - Fracture Clinical Trials

Safety and Exploratory Efficacy Study of UCMSCs in Patients With Fracture and Bone Nonunion

Start date: January 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of the present study is to evaluate the safety and exploratory efficacy of the umbilical cord mesenchymal stem cells for patients with fracture and bone nonunion.

NCT ID: NCT02786498 Completed - Fracture Clinical Trials

Optimal Vitamin D3 Supplementation Strategies for Acute Fracture Healing

Vita-Shock
Start date: November 21, 2016
Phase: Phase 2
Study type: Interventional

The objective is to determine the effect of vitamin D3 supplementation on fracture healing at 3 months.

NCT ID: NCT02698228 Withdrawn - Fracture Clinical Trials

Regional Anaesthesia for Painful Injuries After Disasters

RAPID
Start date: March 2016
Phase: Phase 4
Study type: Interventional

The goal of the RAPID study is to fundamentally transform the way serious injuries are managed after earthquakes and other disasters by introducing a novel and cost-effective method for pain control. The study will enroll patients in the aftermath of a major earthquake to determine whether regional anesthesia, either with or without ultrasound-guidance, can reduce suffering from lower limb injuries, the most common earthquake-related injury, above and beyond the current standard of care for pain control in these settings.

NCT ID: NCT02635022 Recruiting - Osteoporosis Clinical Trials

Fragility Fracture Liaison Service and Anti-osteoporosis Medication Monitoring Service Study

Start date: September 2015
Phase:
Study type: Observational

Aims: (1) to Establish the FLS services at the National Taiwan University Hospital Jinshan Branch. (2) To establish a anti-osteoporosis medication management service at Jinshan Branch. Method: From Aug., 2015, a fracture liaison services (FLSs) following the 13 'Capture the Fracture Best Practice Standards' were implemented at the National Taiwan University Hospital Jinshan Branch health care system. The Jinshan Branch program enrolled patient with 1) new hip fracture 2) newly identified vertebral fractures (radiological or clinical) from both inpatients and outpatients. At the same time, a osteoporosis medication management service is also establish as a complement of FLS to enroll patients on antiosteoporosis medications (AOMs) but not necessary with fracture. Participating physicians will select those eligible for services and refer to study coordinators. Study coordinators will conduct baseline assessments on osteoporosis/fracture risks, record medical conditions, AOMs, provide educations on osteoporosis, fracture, sarcopenia, fall, medications, nutrition, and exercise. They also arrange return clinic visit, telephone reminder and follow up for patients, and communicate with providers on regular bases. During the whole study period, the investigators planed to enroll 200 patients (with or without fracture). Each patient would be assessed at baseline, and every 4 months last for two years.

NCT ID: NCT02608749 Completed - Osteoporosis Clinical Trials

Osteoporosis and Fall Prevention High Risk Population Intervention and Follow up in the Metropolitan Area

Start date: May 2014
Phase: N/A
Study type: Interventional

BACKGROUND: The deterioration of musculoskeletal system imposes significant impact on physical activity in older adults. METHODS: This was a randomized, parallel-group, prospective study. All participants received education program including home-based exercise. The IC group consisted of different modalities of exercise while the LEE group performed machine-based exercise. Body composition, muscle strength, and physical performance were measured at their baseline and 3 months follow-up.

NCT ID: NCT02591043 Completed - Fracture Clinical Trials

Surgical Treatment of Low Energy Pelvic Fractures in the Elderly

PelvicRetro
Start date: October 2015
Phase: N/A
Study type: Interventional

Since May 2010 the Department of Trauma, Basel University Hospital has performed surgical stabilisation of the posterior pelvic ring on 55 patients. These patients have not received a structured follow up examination or evaluation of outcome after surgery.

NCT ID: NCT02481869 Completed - Fracture Clinical Trials

Platelet Rich Plasma Injection in Pilon Fractures

Start date: June 2015
Phase: N/A
Study type: Interventional

Patients who sustain broken ankles have a very high risk of developing arthritis soon after injury (within 2 years). This arthritis can cause increased pain and a decrease level of function, especially if the injury occurs at an early age. During and shortly after ankle injury, there is an inflammatory chemical process that takes place in the ankle that can cause damage to the cartilage in the ankle joint. The investigators want to use what is called Platelet Rich Plasma (PRP), which is produced from a small amount of the patient's own blood, to inject into the injured ankle to see if they can decrease the inflammation that happens after the injury and to see if they can decrease arthritis.