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Fractures, Bone clinical trials

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NCT ID: NCT00470691 Completed - Colles' Fracture Clinical Trials

Dorsal Splint or Circular Cast for Colles' Fracture?

Start date: June 2004
Phase: N/A
Study type: Interventional

At our hospital, all Colles' fractures deemed suitable for conservative treatment are reduced and immobilised with a plaster of Paris dorsal splint which is converted to a complete cast after 10 days. According to individual factors such as age, general health and radiological results after 10 days, some patients with severe redisplacement are readmitted to hospital for surgery. The main purpose of this study is to determine whether, during the first 10 days of immobilisation, a complete plaster cast or a dorsal plaster splint best retains the alignment of a reduced Colles' fracture. In addition, we aim to compare the complication rates of the two methods.

NCT ID: NCT00464230 Completed - Clinical trials for Femoral Neck Fractures

Hemiarthroplasty or Internal Fixation for Displaced Femoral Neck Fractures

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

An estimated 1.6 million patients sustain a hip fracture every year, about half of these are intracapsular femoral neck fractures. A femoral neck fracture is a life changing event for any patient, and the risk of disability, increased dependence and death is substantial. The main treatment options for displaced femoral neck fractures are internal fixation and arthroplasty. It is established that there are more complications and reoperations after internal fixation, but there is no consensus about which procedure that gives best functional results.

NCT ID: NCT00463905 Completed - Osteoporosis Clinical Trials

Evaluation of the Impact of a Case-finding Strategy for Vertebral Fractures

COSHIBA
Start date: October 2007
Phase: N/A
Study type: Interventional

Postmenopausal women with vertebral fractures (VFs) represent an important target for secondary fracture prevention, but few of these patients come for clinical attention. Recent evidence suggests that screening postmenopausal women for clinical risk factors like height loss and fracture risk identifies those at high risk of prevalent VFs who should be referred for diagnostic X-rays, a strategy which is likely to prove cost effective. However, before being applied at a United Kingdom (UK)-wide level, it needs to be established that use of this strategy improves secondary fracture prevention, and that these benefits are achieved in a cost-effective manner. To examine these questions, a randomised-controlled-trial will be performed in which women aged 65-80 from general practitioner (GP)-practices in the intervention group will be invited for risk factor assessment, followed by referral for thoracolumbar X-ray where appropriate. The primary outcome will be a change in bisphosphonate or other drug prescribing between the intervention and control arms after six months.

NCT ID: NCT00460733 Completed - Colles' Fracture Clinical Trials

SOLID-Effect of Risedronate Sodium at Distal Radius in Colle's Fracture.

SOLID
Start date: March 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of risedronate sodium (Actonel®) after a wrist fracture in postmenopausal women.

NCT ID: NCT00438750 Completed - Clinical trials for Distal Radius Fractures

Comparison of Occupational Therapy and Home Exercises for Adults With Operatively Treated Distal Radius Fractures

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

The purpose of this study is to compare to ways of rehabilitating after surgery for distal radius fractures treated operatively with a volar plate.

NCT ID: NCT00438633 Completed - Clinical trials for Proximal Humeral Fractures

Comparison of Early and Late Therapy for Adults With Non-Operatively Treated Proximal Humerus Fractures

Start date: February 2005
Phase:
Study type: Observational

The purpose of the study is to compare two common ways of rehabilitating after proximal humerus fractures treated non-operatively.

NCT ID: NCT00438308 Completed - Clinical trials for Distal Radius Fractures

Comparison of Early and Late Therapy for Adults With Operatively Treated Distal Radius Fractures

Start date: December 2004
Phase: N/A
Study type: Observational

The purpose of the study is to compare two common ways of rehabilitating after surgery for distal radius fractures treated operatively with a volar plate.

NCT ID: NCT00429585 Completed - Tibial Fractures Clinical Trials

A Multicenter Randomized Trial Comparing IM Nails and Plate Fixation in Proximal Tibial Fractures

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

This study looks at two types of surgical treatments and hopes to answer the question: which is the best way to surgically treat a proximal tibia fracture? Both procedures being studied are standard of care (used routinely) and use FDA approved devices. All medical and surgical treatment will be the same for participants as non-participants.

NCT ID: NCT00424619 Completed - Hip Fracture Clinical Trials

A Randomised, Controlled Comparison of Vitamin D Strategies is Acute Hip Fracture Patients

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

The purpose of the study is to determine the best dose of Vitamin D to give to hip fracture patients to achieve the optimal therapeutic level.

NCT ID: NCT00416039 Completed - Fractures Clinical Trials

Efficacy of Sublingual Midazolam in Association With Oral Morphine in Children Analgesia After Bone Fracture

MIDAZODOL
Start date: January 2007
Phase: Phase 3
Study type: Interventional

It is a randomized simple-blind monocentric study; the group A will receive oral morphine with placebo and the group B will receive oral morphine with sublingual midazolam. The aim of this study is to show a more important pain decrease in the group taking midazolam versus placebo.