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Fractures, Bone clinical trials

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NCT ID: NCT03060876 Recruiting - Clinical trials for Proximal Humerus Fracture

Hanover Humerus Registry

HHR
Start date: June 2016
Phase: N/A
Study type: Observational [Patient Registry]

This register study collects data of patients with proximal humerus and humerus shaft fractures to monitor the healing process by assessing shoulder function and quality of life according to the treatment method (operative or conservative management).

NCT ID: NCT03059368 Completed - Tibial Fractures Clinical Trials

New Bone Fixation Plate for the Repair of Tibial Avulsion Fracture of Posterior Cruciate Ligament of the Knee

Start date: August 2013
Phase: N/A
Study type: Interventional

To construct a self-designed plate fixation device for posterior cruciate ligament reconstruction, aim to verify its advantages on anatomical knee stability, so as to achieve fracture healing and keep tension after posterior cruciate ligament reconstruction.

NCT ID: NCT03056950 Recruiting - Rehabilitation Clinical Trials

BFR DISTRAD NON OP: Blood Flow Restricted Training During Rehabilitation Following Distal Radius Fracture

Start date: March 2016
Phase: N/A
Study type: Interventional

Occlusion training, resistance exercise performed with a specialized venous tourniquet, leads to beneficial changes in muscle strength at low resistance and minimal stress on the nearby joint. This novel resistance training has the potential to greatly improve muscle strength gains in individuals who are unable, for medical reasons, to perform the high resistance exercises typically required to improve strength. Our study will examine the effect of this technique on strength recovery following distal radius fracture treated with cast immobilization (non-operatively). The primary objective of the intervention is to achieve accelerated recovery of forearm, wrist and hand function as assessed using measures such as grip/pinch strength, validated questionnaires, and functional outcome testing. Occlusion training can potentially serve as a specialty intervention for rehabilitation patients, reduce the cost of care, and improve the treatment options for both patients and providers.

NCT ID: NCT03044015 Recruiting - Clinical trials for Osteoporotic Fractures

Primary Care Based Intervention for the Secondary Prevention of Osteoporotic Fractures

APROP
Start date: January 2017
Phase: N/A
Study type: Interventional

BACKGROUND Recent evidence has been published about the effectiveness for the secondary prevention of osteoporotic fractures (OF) of the hospital-based fracture liaison services. AIM To assess the effectiveness of a primary care based intervention in the secondary prevention of OF. METHODOLOGY Prospective study of random clusters, defined at the primary-care trust (PCT) level. Total study follow-up 3 years. Sample size 1800 patients. DESCRIPTION To launch a defined strategy for the identification of OF. To carry out a primary care based intervention about lifestyle, diet and drug prescription, if needed, with an intensive follow-up in the intervention PCT vs treatment as usual in the control branch. ANALYSIS As the outcome are the new OF, a survival analysis will be done. Risk factors will be analyzed through Cox proportional hazard regression model stratified by age groups. Outcomes : - new OF ratio in intervention vs control areas. - maintenance of the adherence to the pharmacological and non pharmacological interventions proposed - assessment of cost-effectivity of the intervention

NCT ID: NCT03042546 Terminated - Clinical trials for Open tíbia Fracture With Sub-segmental Bone Loss

Calcium Sulfate Spacer in Open Tibia Fractures

Start date: February 1, 2017
Phase: Phase 4
Study type: Interventional

Investigators will compare antibiotic impregnated Calcium sulfate versus PMMA versus nothing in these sub-segmental bone defects.

NCT ID: NCT03042533 Terminated - Clinical trials for Closed Transverse Fracture of Shaft of Tibia

Union Rate of Transverse Tibia Fracture

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

The investigators will compare the three methods of seating a tibial nail - Backslapping or Backslapping with Dynamic Locking or Internal Compression.

NCT ID: NCT03040739 Completed - Acetabulum Fracture Clinical Trials

Treatment of Acetabulum Fracture With O'ARM Surgical Imaging

Start date: July 8, 2016
Phase: N/A
Study type: Observational [Patient Registry]

Acetabulum fracture are high energy trauma in young people as it can be the result of a simple fall in elder people. This fracture generates an incongruity between acetabulum and femoral head. So surgery is recognized as the best treatment even if technically difficult because of the the complexity of anatomy.Navigation is widely used in orthopaedic surgery . The aim of the study is to evaluate the effect of peroperative navigation system on reduction of the acetabulum articular surface

NCT ID: NCT03035942 Completed - Pruritus Clinical Trials

Quality of Recovery After Dexamethasone, Ondansetron or Placebo Intrathecal Morphine Administration

Start date: January 2, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate not only the occurrence of side effects, but the quality of the recovery (QoR-40 Questionnaire) of patients submitted to spinal anesthesia with administration of low doses (0.1 mg) of intrathecal morphine for the surgical treatment of fractures in one of the lower limbs and who will receive prophylactic ondansetron (4mg), dexamethasone (8mg) or placebo.

NCT ID: NCT03032653 Completed - Surgery Clinical Trials

Immediate Weight-Bearing Ankle Study

Start date: February 9, 2017
Phase: N/A
Study type: Interventional

This single-centre historical control group comparative study will compare outcomes of surgically-treated rotational ankle fractures and the current routine practice of early protected weightbearing and range of motion with immediate unprotected weightbearing as tolerated and range of motion after ankle open reduction and internal fixation.

NCT ID: NCT03031509 Not yet recruiting - Nonunion Fracture Clinical Trials

Treatment of Nonunion of Limb Fracture With Human Amniotic Epithelial Cells(hAECs)

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

The purpose of this study is to evaluate the efficacy and safety of human amniotic epithelial cells transplant in nonunion of limb fracture patients.