Clinical Trials Logo

Fractures, Bone clinical trials

View clinical trials related to Fractures, Bone.

Filter by:

NCT ID: NCT00323232 Completed - Hip Fracture Clinical Trials

Comparison of Treatment Outcomes in Hip Fractures Surgically Fixed With Either a Two or Four Hole Device.

Start date: December 2010
Phase: Phase 4
Study type: Interventional

Although Standard of Care for Hip Fractures is the Device (Dynamic Hip Screw) being studied in this project, and both sizes (the 2 and the 4 hole versions) are currently in use there is not widespread agreement yet whether there is an optimal number of screws (2 or 4) required for the best outcomes. If it can be shown that a 2 hole version is just as successful in outcomes it would allow for a smaller incision (surgical cut) at the site of the fracture. This could reduce soft tissue dissection, operating time, and surgical blood loss. This in turn would reduce post operative pain, blood loss, and hospital length of stay.

NCT ID: NCT00299052 Completed - Open Fracture Clinical Trials

Efficacy of DBM on Fractures of the Shinbone (Tibia)

Start date: March 2006
Phase: Phase 4
Study type: Interventional

The Tibia bone (shinbone) is located in the leg, itis the most frequently fractured bone in the body and has very poor blood supply because it is surrounded by skin and fat instead of muscle like the thighbone causing healing problems. Problems frequently found during the healing process are malunion (bone heals in the wrong place), nonunion (the bone never heals), and compartment syndrome (a big inflammation of muscle that causes compression of nerves and blood vessels) with necrosis (death) of tissue. Surgeons have tried to decrease these problems by using different surgical techniques and substances to accelerate healing. Substances frequently used in fractures are bone grafts. Bone grafts are normally obtained from the wrist or the hip bone, and sometimes can cause other complications varying from pain to infection. To avoid complications, investigators have used alternatives such as obtaining bone from donors. The donor bone grafts are carefully analyzed and cleaned to ensure they will not cause problems for the receiver. Bone obtained from donors is called Demineralized Bone Matrix (DBM). DBM has proved to be very effective in helping fractures to heal faster and we want to use it in patients with tibia fractures. This study is important because DBM can improve the way tibia fractures are treated and could have the potential to decrease the time patients must stay in the hospital. DBM could improve healing time and diminish overall costs. Also, with the use of DBM plus reamings, patients will have fewer complications like pain and infection.

NCT ID: NCT00285961 Completed - Wounds and Injuries Clinical Trials

Evaluation of Cork Splint Materials Instead of Plaster Splint for Children

Start date: n/a
Phase: N/A
Study type: Interventional

This is an evaluation of the functionality and added value of cork splint materials instead of a plaster splint for children (3-11 years old).

NCT ID: NCT00283998 Completed - Clinical trials for Odontoid Fractures Type II

Comparing Surgical to Conservative Management in the Treatment of Type II Odontoid Fractures Among the Elderly

Start date: January 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the safety and effectiveness of surgical versus conservative management of type II odontoid fractures among patients >/= 65 years of age. Of secondary interest is to determine if there are differences in outcomes between anterior screw fixation and posterior fusion of these fractures.

NCT ID: NCT00280943 Completed - Osteoporosis Clinical Trials

Secondary Prevention of Osteoporotic Fractures in Residents of Long-Term Care Facilities

Start date: January 2005
Phase: Phase 2/Phase 3
Study type: Interventional

Osteoporotic fractures of the hip are a major cause of admission to long-term care facilities. Such fractures put patients at high risk for further fractures, pain and disability. Current data show that many patients in long-term care facilities do not receive FDA medications for their osteoporosis. This trial will test whether a multi-model intervention (which provides feedback about provider use of osteoporosis medications, information about osteoporosis, and currently approved osteoporosis medications)directed at physicians, other health care providers, and nurses will improve the number of prescriptions written for FDA approved medications for osteoporosis treatment.

NCT ID: NCT00280267 Completed - Muscle Weakness Clinical Trials

Testosterone Therapy After Hip Fracture in Elderly Women

Start date: August 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the feasibility of testosterone replacement therapy in frail elderly female hip fracture patients who have testosterone deficiency, and to obtain preliminary information about the effects of testosterone therapy on muscle strength and size, bone density, mobility, daily functioning, and quality of life.

NCT ID: NCT00274378 Completed - Radius Fractures Clinical Trials

Allomatrix Injectable Putty in Distal Radius Fractures

Start date: June 2005
Phase: Phase 4
Study type: Interventional

Allomatrix is a combination of Demineralized Bone Matrix with a binding medium of calcium sulfate hemihydrate and carboxymethylcellulose. Allomatrix combines the osteoinductive capacity of DBM with the osteoconduction and controlled resorption of surgical grade calcium sulfate. Unstable fractures of the distal radius do not resist displacement once it has been manipulated into an anatomical position. There is a parallel between the quality of the anatomic result and the residual capacity of the wrist, except in older, low demanding patients. Injectable osteoconductive cements have been introduced to fill voids in metaphyseal bone and may provide a better stability around hardware in osteoporotic bone and help maintain reduction of fracture fragments.Moreover, a product like ALLOMATRIX could accelerate and improve bone healing and fracture stability by its osteoinductive properties. However, the clinical significance of these new bone graft materials still have to be proven in a randomised controlled study set-up.

NCT ID: NCT00264511 Completed - Tibial Fracture Clinical Trials

Hyperbaric Oxygen in Lower Leg Trauma

Start date: February 13, 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Study hypothesis :Hyperbaric Oxygen may prevent complications and improve outcomes in severe lower limb trauma. We propose to investigate this hypothesis by conducting an International multi centre randomised control trial of standard trauma/orthopaedic care with or without a concurrent course of hyperbaric oxygen treatments.

NCT ID: NCT00254631 Completed - Fractures Clinical Trials

Preemptive Analgesia With OxyContin Versus Placebo Before Surgery for Long Bone Fractures

Start date: April 2007
Phase: Phase 4
Study type: Interventional

We would like to check whether pre-operative administration of an oral controlled-release opioid formulation (Oxycodone hydrochloride (OxyContin)) could result in a clear effect of preemptive analgesia.

NCT ID: NCT00254514 Completed - Bone Fracture Clinical Trials

Controlled Study to Evaluate the Efficacy and Safety of the Treatment With Growth Hormone in Tibia Fractures

Start date: August 2001
Phase: Phase 2
Study type: Interventional

This trial is conducted in Africa, Europe and Middle East. This trial investigates the efficacy and safety of three dose levels of Norditropin® (growth hormone) as compared to placebo in the treatment of tibia fractures. The trial will be conducted in two parts: in the first part, the patients will be evaluated with regard to efficacy (fracture healing) and safety at short time intervals until week 24 post-surgery. In the second part, long-term safety and fracture healing up to 12 months post-surgery will be evaluated.