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Hip Fractures clinical trials

View clinical trials related to Hip Fractures.

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NCT ID: NCT02247791 Active, not recruiting - Hip Fractures Clinical Trials

Uncemented Compared to Cemented Femoral Stems in Total Hip Arthroplasty

CHANCE
Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether an uncemented hip prosthesis is as safe as an cemented hip prosthesis for patients undergoing total hip arthroplasty surgery following a displaced femoral neck fracture.

NCT ID: NCT01352754 Active, not recruiting - Hip Fracture Clinical Trials

Troponin T Elevation in Patient Undergoing Hip Fracture Surgery

Start date: April 2011
Phase: N/A
Study type: Observational

Background: Patients undergoing hip fracture surgery are elderly and usually have co-morbidities; hence they are at risk for perioperative MI. Troponin is the gold standard for diagnosis of myocardial damage and currently the cornerstone of MI diagnosis. Perioperative troponin elevation is a poor prognosis factor. The significance of minor troponin elevation, detected by highly sensitivity troponin T assay, is unknown. Objectives: To determine the frequency of perioperative troponin T elevation using highly sensitivity troponin T assay, and to determine the clinical significance of this elevation. Methods: Serum Troponin T levels of patients undergoing hip fracture surgery will be tested prior to surgery 48 hrs and 72 hrs after surgery, using highly sensitivity troponin T assay. Patients will be followed for 1 year. Primary outcomes- The number of patients with elevated troponin levels perioperatively and cardiac mortality at 3 months, 6 months and 1 year.

NCT ID: NCT01129219 Active, not recruiting - Exercise Clinical Trials

Observation and Progressive Strength Training After Hip Fracture

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

This is a randomized, controlled; single-blind parallel group trial carried out with hip fracture patients, starting at 12 weeks post fracture. Patients were approached during their acute stay in hospital, followed without any extra intervention for 12 weeks, and then randomized in a 2:1 manner to either intervention or control for the next 12 weeks. After the first 12 weeks intervention the intervention group were divided into two groups and randomized to an new single-blind parallel group trial for further intervention.

NCT ID: NCT01017341 Active, not recruiting - Hip Fracture Clinical Trials

Hip Protector for Prevention of Hip Fracture

Start date: June 2010
Phase: Phase 3
Study type: Interventional

This study aims to evaluate the efficacy of the investigators PSU hip protector for prevention of fracture in elderly.The eligible patients include those with previous diagnosed as unilateral hip fracture. They will be randomized into 2 groups;psu hip protector and no protector. The patients will be instructed to wear the protector fulltime.The inceidence of hip fracture will be compared between both group at the end of 1 year.

NCT ID: NCT00859378 Active, not recruiting - Hip Fracture Clinical Trials

Cemented vs Non-cemented Semiendoprosthesis in the Treatment of Proximal Femoral Fractures

Start date: October 2008
Phase: N/A
Study type: Interventional

The hip semiendoprosthesis is an acceptable method to treat the proximal femoral fractures. Traditionally, the cemented version of the semiendoprosthesis has been used for this indication. However, the cementing carries a risk of fat embolism during the pressurization of the cement. The fat embolism can be avoided when using the non-cemented semiendoprosthesis. In this study we want to find out whether there are any differences in the treatment results between the cemented and non-cemented semiendoprostheses when treating the proximal femoral fractures.

NCT ID: NCT00800644 Active, not recruiting - Cervical Cancer Clinical Trials

Pelvic Fractures and Radiation Therapy for Cervical Cancer

Start date: November 5, 2008
Phase:
Study type: Observational

The goal of this study is to estimate how often pelvic fractures occur in women treated with radiation therapy for either newly diagnosed or recurrent cervical, endometrial, or vaginal cancer. The study will also estimate the changes in bone mineral density and the changes in the blood that relate to "bone turnover". High bone turnover can weaken bones and make you more likely to break a bone.

NCT ID: NCT00414830 Active, not recruiting - Osteoporosis Clinical Trials

Systematic Prevention of Further Fractures in Patients With Hip Fractures and Osteoporosis.

Start date: January 2005
Phase: N/A
Study type: Observational

The purpose of this study is to determine if prevention of further fractures is possible through systematic evaluation for osteoporosis in patients with recent hip fracture

NCT ID: NCT00345488 Active, not recruiting - Hip Fracture Clinical Trials

Fast Track Admittance of Hip Fracture Patients

Start date: September 2002
Phase: Phase 4
Study type: Observational

The study examines time spent in the emergency room on admission of patients with hip fracture in a cohort with a traditional setup compared with a prospective cohort with a fast track admission schedule including nurse initiation of treatmnet, standardized analgesia, fluid and oxygen therapy and standardized logistics for x-ray and admission procedures.

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.