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Hip Fracture clinical trials

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NCT ID: NCT00286936 Terminated - Delirium Clinical Trials

Incidence of Delirium in Hip Fracture Patients Randomized to Regular Hypnotics vs Placebo

Start date: February 2004
Phase: Phase 4
Study type: Interventional

To examine the influence of regular hypnotic therapy on the incidence of delirium after hip fracture surgery

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: NCT00250237 Completed - Hip Fracture Clinical Trials

Post-operative Haloperidol Versus Placebo for Prevention of Post-operative Delirium After Acute Hip Surgery

Start date: November 2005
Phase: Phase 3
Study type: Interventional

In this study the investigators want to determine if treatment with haloperidol direct post-operatively after acute hip surgery in high risk patients protects against developing a post-operative delirium.

NCT ID: NCT00197496 Completed - Hip Fracture Clinical Trials

Body Weight Supported Treadmill Training Following Hip Fracture

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

Achieving independent ambulation is an important goal of hip fracture rehabilitation, as it is predictive of returning to the community and of future health problems. Current research regarding post-hip fracture rehabilitation is sparse. Body weight supported treadmill training (BWSTT) is a novel approach to retrain walking abilities. BWSTT may be ideal for retraining walking after hip fracture, as it is task-specific and alleviates the demands of maintaining balance while walking skills are trained. The use of the harness may provide a sense of security for the patient, facilitating walking training. The proposed project will investigate the feasibility and tolerability of BWSTT after hip fracture, and its impact on function, mobility, quality of life and fear of falling. It is hypothesized that BWSTT 3-5 times weekly in acute hip fracture patients will improve function, mobility, quality of life and reduce fear of falling.

NCT ID: NCT00175175 Completed - Osteoporosis Clinical Trials

Randomized Trial of Osteoporosis Intervention Strategies in Hip Fracture Patients

Start date: March 2002
Phase: N/A
Study type: Interventional

Patients with hip fractures have suffered the most devastating consequence of osteoporosis; and yet, they are rarely if ever tested or treated for the condition, even though they remain at high risk of recurrent fracture. We hypothesize that, compared with usual care, an allied health professional-run osteoporosis service (case management) will be able to increase testing and treatment of osteoporosis in patients at high risk of fracture.

NCT ID: NCT00162630 Completed - Hip Fracture Clinical Trials

Fascia Iliaca Compartment Blockade as Analgesia for Hip Fractures in the Acute Phase

Start date: May 2003
Phase: Phase 4
Study type: Interventional

To evaluate the analgesic potential of an neural blockade (Fascia iliaca compartment) with local anaesthetics in patients with hip fracture immediately after arrival in the emergency department.

NCT ID: NCT00162617 Active, not recruiting - Hip Fracture Clinical Trials

The Effect of Liberal vs. Restrictive Transfusion Strategies on Rehabilitation After Hip Fracture Surgery

Start date: January 2004
Phase: Phase 4
Study type: Interventional

To examine the effect of two different transfusion regimens on rehabilitation after hip fracture surgery.

NCT ID: NCT00128115 Terminated - Hip Fracture Clinical Trials

Treatment of Sarcopenia in Post-Hip Fracture Patients (0677-032)

Start date: September 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to demonstrate an improvement in physical functional recovery, following administration of Drug for 24 weeks, in patients who have recently experienced a hip fracture. This study will also evaluate the safety and tolerability of Drug. This is an early phase trial and some specific protocol information is proprietary and not publicly available at this time. (Full information is available to trial participants).

NCT ID: NCT00046254 Completed - Osteoporosis Clinical Trials

Evaluating the Ability of Zoledronic Acid to Reduce the Rate of Subsequent Osteoporotic Fractures After a Hip Fracture

Start date: February 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether zoledronic acid given once yearly for two years to men and women after surgical repair of a recent hip fracture will significantly reduce the rate of all re-occurring (new) osteoporotic fractures. All patients will receive vitamin D and calcium.

NCT ID: NCT00022802 Terminated - Hip Fracture Clinical Trials

Image Guided System for Orthopaedic Surgery

Start date: December 2002
Phase: Phase 2
Study type: Interventional

This project focuses on the further development and clinical testing of an image-guided surgical system. The system will help surgeons perform procedures that involve inserting a screw, guide pin, drill bit, or other straight object into bone-for example, inserting screws in a broken hip bone. These surgeries are currently done with the help of a mobile x-ray device called a C-arm, which provides the surgeon with x-ray images during the procedure. C-arms have some disadvantages, including image distortion, radiation exposure, and the need for time-consuming adjustments of the C-arm during the surgery. The new method would deal with these shortcomings with a computer-based system that adds to the existing C-arm system. It would provide the surgeon with a real-time view of the insertion process, and could improve the accuracy and speed of certain surgical procedures. Disadvantages associated with C-arms include image distortion, radiation exposure, and time consuming reconfiguration of the C-arm during the insertion process. The proposed system would address these shortcomings with a computer-based system that augments the existing C-arm system.