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Fractures, Bone clinical trials

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NCT ID: NCT02150980 Completed - Clinical trials for Fractures or Dislocations

INternational ORthopaedic MUlticenter Study in Fracture Care (INORMUS)

INORMUS
Start date: April 2014
Phase:
Study type: Observational

Background: Worldwide, injuries from trauma represent a major public health problem. The World Health Organization (WHO) has deemed this problem as one of the most important global priorities, calling 2011-2020 the 'Decade of Action for Road Safety'. Despite this, there is little empirical data in low and middle-income countries quantifying the burden of musculoskeletal injuries. Methods: INORMUS is a global, prospective, multi-center, observational cohort study. The primary objective of the study is to determine the mortality, re-operation and infection rates of musculoskeletal trauma patients within 30 days post-hospital admission. The INORMUS study seeks to enroll 40,000 patients from low-middle income countries in Africa, Asia, and Latin America.

NCT ID: NCT02150850 Recruiting - Clinical trials for Atypical Femur Fracture

Quebec Registry for Atypical Femur Fractures

Start date: April 2012
Phase:
Study type: Observational [Patient Registry]

Bisphosphonates are recommended as first-line agents to reduce fracture risk in patients with osteoporosis and have in general an excellent safety profile. However, recent reports have noted that prolonged use of bisphosphonates may be associated with rare but serious adverse effects, namely atypical femur fractures (AFF), an atraumatic subset of subtrochanteric and diaphyseal fractures. The overarching aim of this project is to contribute to the characterization of clinical, biomechanical, radiological and genetic predictors of AFF, associated or not with bisphosphonate and-or denosumab therapy. AFF arise on the lateral (external) aspect of the subtrochanteric and diaphyseal regions of the femur, regions subjected to high mechanical loads. Because of this unique distribution, the investigators hypothesis is that patients with AFF demonstrate specific geometrical variations of their femur whereby baseline tensile forces applied to the lateral cortex are higher and might favour the appearance of these rare stress fractures. Measurements to investigate these geometric variations with be calculated from 3D images reconstructed using scans procured using the EOS® low irradiation 2D-3D X-Ray scanner.

NCT ID: NCT02150720 Completed - Hip Fracture Clinical Trials

Prevention of Postoperative Bleeding in Subcapital Femoral Fractures

TRANEXFER
Start date: February 2013
Phase: Phase 3
Study type: Interventional

The main hypothesis of this clinical trial is that the use of intra-articular tranexamic acid and the fibrin glue plus usual hemostasis will reduce at least a 25% the postoperative blood loss with respect to usual hemostasis in patients undergoing subcapital femoral fractures.

NCT ID: NCT02148848 Recruiting - Clinical trials for Osteoporotic Fractures

Short-term Functional Recovery Between Early- and Late Bisphosphonate Treatment Following Hemiarthroplasty

Start date: June 2013
Phase: Phase 4
Study type: Interventional

Femoral neck fracture in the elderly is one indication for initiating osteoporosis treatment. Bisphosphonates remain the first line therapy; however, many orthopaedic surgeons concern regarding their effects on fracture healing process. Therefore, therapy is usually delayed for a period of time. To the best of our knowledge, there is no scientific data to support whether bisphosphonate treatment should be given immediately after the surgery or it should be delayed.

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: NCT02133794 Not yet recruiting - Hip Fracture Clinical Trials

Tomosynthesis Use in Detecting Subtle Occult Hip Fractures

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

The purpose of this project is to determine if using tomosynthesis, in conjunction with x-ray, is better at detecting hip fractures than using x-ray alone. The goal of this study will be to include the use of tomosynthesis with x-ray as usual practice when a patient comes to the emergency room with symptoms of a hip fracture.

NCT ID: NCT02131571 Completed - Vertebral Fractures Clinical Trials

Prevalence of Vertebral Fractures in HIV Infected Patients Older Than 50 Years

FractaVIH
Start date: June 30, 2014
Phase:
Study type: Observational

Prospective cohort study to determine the prevalence of vertebral fractures in HIV infected patients older than 50 years.

NCT ID: NCT02129270 Completed - Clinical trials for Fractures of the Distal Radius

Hematoma Block for Reduction of Distal Radius Fractures

Start date: May 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to Prove that injection of 15 to 20 mL of lidocaine 1% into the fracture site (Hematoma block) is more effective in terms of pain relieving then injection of 10 mL of lidocaine 2%, and equally safe in terms of complications, for closed reduction of distal radius fractures.

NCT ID: NCT02114840 Recruiting - Surgery Clinical Trials

Pronator Quadratus Preservation Following Volar Plate Fixation. RCT

PROQUAP
Start date: April 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine pronator quadrutus preservation have clinical impact following volar plate fixation

NCT ID: NCT02106442 Completed - Osteoporosis Clinical Trials

36-month Special Drug Use Surveillance on Frequency of Bone Fractures With Sodium Risedronate 75 mg Tablets

Start date: May 13, 2013
Phase:
Study type: Observational

The purpose of this survey is to evaluate the effectiveness (endpoints: frequency of bone fractures, percent change in bone density, etc.) and safety of administration of sodium risedronate tablets 75 mg for 36 months in osteoporosis patients in daily medical practice.