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Hip Fractures clinical trials

View clinical trials related to Hip Fractures.

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NCT ID: NCT00133640 Recruiting - Hip Fractures Clinical Trials

Early Rehabilitation After Hip Fracture

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

The aim of this study is to compare a low versus high intensity physiotherapy early rehabilitation program combined with a low versus high dose vitamin D early rehabilitation program in a randomized controlled trial among elderly patients with acute hip fracture in an acute care setting. The primary outcome to be compared between treatment arms is the rate of falls during a 12-month follow-up. Secondary outcomes are injurious falls, number of persons who fell, low-trauma fractures (at the hip, forearm, humerus, pelvis, ankle, spine, femur, tibia), disability, quality of life (Euro-Qol), mortality and health care utilization. Another secondary outcome will be admission to nursing home compared between treatment arms among subjects, who are community-dwelling prior to the index hip fracture. Admission to nursing home is the marker of loss of independence for the individual, but also triggers high cost for the society. The study will provide new early rehabilitation guidelines to allocate health care resources efficiently in the acute care setting. Eventually and most importantly, the study will help improve outcomes in patients with hip fractures.

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: NCT00119457 Completed - Clinical trials for Venous Thromboembolism

Factor IX Inhibition in Thrombosis Prevention (The FIXIT Trial)

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

The purpose of this study is to determine whether TTP889 prevents venous thromboembolism following surgery to repair hip fracture.

NCT ID: NCT00058864 Completed - Hip Fractures Clinical Trials

The HIP Impact Protection Program (HIP PRO)

Start date: September 2001
Phase: N/A
Study type: Interventional

HIP PRO is a multicenter randomized, controlled trial of an energy absorbing and distributing padding system designed to reduce the incidence of hip fractures in 546 nursing home (NH) residents. The trial is being conducted in three geographic regions of the US: Boston, St. Louis, and Baltimore. Non bed- or chair-bound residents over the age of 65 are given protective underwear containing a single pocket and hip pad so that each resident becomes his/her own control. During the trial, hip fracture incidence will be compared in padded and unpadded hips using an intent to treat analysis. A secondary aim is to identify resident and facility factors contributing to non-adherence with the use of the hip protector.

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.

NCT ID: NCT00006194 Completed - Hip Fractures Clinical Trials

Effects of Exercise on Markers of Inflammation in Skeletal Muscle in Elderly Hip Fracture Patients

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

Decreased skeletal muscle mass is a prevalent condition among the elderly, and an important cause of disability and functional decline. The declines in muscle mass associated with aging may be related to alterations in specific kinds of growth factors in the muscle. Elderly hip fracture patients often have significant decreases in muscle mass. The purpose of this study is to investigate whether an exercise program can induce changes in muscle growth factors that are associated with increases in muscle mass and strength in elderly hip fracture patients.

NCT ID: NCT00000436 Completed - Clinical trials for Unilateral Hip Fracture

Improving Functional Recovery After Hip Fracture

Start date: July 1993
Phase: Phase 3
Study type: Interventional

This project will assess the effectiveness of a novel approach involving patient education and strength training to improve functional recovery after a hip fracture. Participants will be randomly assigned to one of two study groups. One group (control group) will receive standard medical care. The other group will participate in a program of patient education and strength training, including an at-home walking program.