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Fracture clinical trials

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NCT ID: NCT01605240 Recruiting - Pain Clinical Trials

Ibuprofen Versus Codeine. Is One Better for Post-operative Pain Relief Following Reduction of Paediatric Forearm Fractures?

Start date: July 2012
Phase: N/A
Study type: Interventional

For simple fractures treated in the emergency department with cast immobilisation only, ibuprofen has been shown to be superior to, or a least or equivalent to codeine with less side effects. These and other studies have commented that their results may not be applicable to children who have fractures that require reduction. There is currently no literature on the management of postoperative pain following reduction of paediatric fractures. The investigators aim therefore is to investigate whether either of the two most commonly prescribed analgesics is superior to the other for postoperative pain management following closed reductions of paediatric forearm fractures. Also, if one agent has more side effects than the other.

NCT ID: NCT01574833 Completed - Fracture Clinical Trials

Early Application of Pulsed Electromagnetic Field in the Treatment of Postoperative Delayed Union

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

The investigators hypothesized that early applied pulsed electromagnetic field treatment on delayed union might lead to increased rate of fracture union and shortened period of treatment.

NCT ID: NCT01544725 Completed - Fracture Clinical Trials

Ketamine-propofol Versus Ketamine Alone for Procedural Sedation in Adults

Start date: April 2012
Phase: Phase 4
Study type: Interventional

Using Ketamine for procedural sedation in adults is often uncomfortable for emergency physicians because of the significant proportion of patients experimenting recovery agitation. The investigators believe that combining propofol to ketamine, the proportion of recovery agitation will be significantly lowered. The objectives of this double-blinded, randomized controlled trial are to compare the proportion of recovery agitation in adults receiving procedural sedation with ketamine-propofol versus ketamine alone, and to compare the proportion of other classical procedural sedation side-effects and parameters such as respiratory depression, hypotension, sedation duration, time of recovery, procedural failures, and levels of satisfaction.

NCT ID: NCT01537523 Not yet recruiting - Fracture Clinical Trials

To Investigate the Effect of Early Community-care Program on Fracture Hip Patient

Start date: February 2012
Phase: N/A
Study type: Interventional

The early community-care program is well-known rehabiliation for the fracture hip patient. For the discharged fracture hip patient from hospital, it is worth to investigate the effect of early mobilization program to improve their physical and psychological aspects.

NCT ID: NCT01514097 Recruiting - Fracture Clinical Trials

Adequacy of Pain Management for Upper Extremity Fracture After Discharge From a Pediatric Emergency Depart

Start date: February 2012
Phase: N/A
Study type: Observational

Pain is a common cause for children seeking care in the Emergency Department (ED). Children with orthopedic injuries often require pain control when seeking emergency care. Despite the high prevalence of ED visits requiring pain control, pain is often poorly assessed and treated in ED settings. Currently, no standard of care exists for the management of this fracture-related pain in children discharged from the ED. Furthermore, discrepancies in analgesia administration to patients of various racial groups seeking emergency care have been documented but are poorly understood. No research currently exists comparing pain severity between upper extremity fractures requiring simple splinting to those treated with sedated reduction and splinting. Furthermore, there is no research regarding the prevalence of significant post-discharge pain nor the differences among ethnic and age groups treated in the ED. Research Questions: What is the prevalence of significant post-discharge pain in children treated for upper extremity fractures? Is there a difference in severity between those children requiring reduction versus simple splinting? Is there a difference in pain severity noted among different ethnic or age groups? Design This is a prospective, un-blinded, observational study that will include patients seeking treatment for an upper extremity fracture.

NCT ID: NCT01395303 Completed - Stroke Clinical Trials

Polymorphisms in the Vitamin D System and Health

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

Polymorphisms in the vitamin D system appear to affect the serum 25(OH)D levels. If so one would expect these polymorphisms to be associated with vitamin D related conditions and diseases, which will be tested in the present study including DNA analyses in 9700 subjects

NCT ID: NCT01343693 Completed - Tumor Clinical Trials

MaxAn Post Market Surveillance Validation

MaxAn
Start date: June 2011
Phase:
Study type: Observational

This study is being performed to document the outcomes of subjects using our MaxAn Anterior Cervical Plate and assess them for Adjacent level Disease. All subjects will be followed for 2 years.

NCT ID: NCT01248182 Terminated - Fracture Clinical Trials

Bone to Skin Thickness Study: Obese Versus Normal Population

Start date: September 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine the bone to skin depth for groups of lean, obese and morbidly obese patients. This information will be potentially helpful with implant design for obese and lean patients.

NCT ID: NCT01242982 Terminated - Fracture Clinical Trials

Subcapital and Shaft Fractures of the 5. Metacarpal

Start date: January 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to find out the best treatment for subcapital and shaft fractures of the 5. metacarpal. It is a prospective randomized multicenter study. Comparing only fractures dislocated more than 30 degrees. One group will be operated with intramedullary pins and one group will be treated conservatively with reduction and then Plaster of Paris for 3 weeks. All patients will be followed up after 3, 6 and 12 months.

NCT ID: NCT01199653 Completed - Fracture Clinical Trials

Study Comparing Plate Stabilization to Conservative Treatment in Midshaft Clavicle Fractures

Start date: August 2004
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to find whether to operate or treat conservatively dislocated midshaft clavicle fractures.