Clinical Trials Logo

Fractures, Bone clinical trials

View clinical trials related to Fractures, Bone.

Filter by:

NCT ID: NCT02202122 Withdrawn - Clinical trials for Femoral Neck Fracture

Interest of the OSA (Obstructive Sleep Apnea) Predictive Scores in the Prognosis of Postoperative Mortality of Femoral Neck Fractures

Start date: September 2014
Phase: N/A
Study type: Observational [Patient Registry]

Interest of the four major OSA Predictive Scores (STOP-BANG, P-SAP, DES-OSA, OSA50) in the prognosis of postoperative mortality after femoral neck fracture.

NCT ID: NCT02198820 Withdrawn - Clinical trials for Femoral Neck Fractures

Practice Survey on Femoral Neck Fractures and the Incidence of Type of Anesthesia on Patient Outcome

Start date: October 2014
Phase: N/A
Study type: Observational [Patient Registry]

Inclusion of all patients with femoral neck fracture presenting in Saint-Luc Bouge Hospital between October 1th 2014 and September 30th 2015. Comparison of severity scores of these patients and the scale of Nottingham on immediate (day 1 and day 2) and late (1 month) outcome.

NCT ID: NCT02198768 Completed - Ankle Fractures Clinical Trials

Ankle Fracture vs Ankle Fracture-Dislocation

Start date: September 2012
Phase:
Study type: Observational

The purpose of this study is to compare outcomes of patients with an ankle fracture to those with ankle fracture-dislocations. We hypothesize that long-term clinical outcomes for patients sustaining ankle fracture dislocations are poorer than those without dislocation.

NCT ID: NCT02196311 Withdrawn - Clinical trials for Supracondylar Humerus Fractures

Treatment Of Supracondylar Fractures Closed Reduction And Circular Ring External Fixation Versus Open Reduction and Internal Fixation

Start date: March 2014
Phase:
Study type: Observational

Patients treated with circular external fixation will have better outcomes (as measured by range of motion (ROM), alignment, outcome surveys) than those treated with open reduction and internal fixation (ORIF).

NCT ID: NCT02194660 Active, not recruiting - Osteoporosis Clinical Trials

Fragility Fracture Liaison Service Project

Start date: January 2014
Phase:
Study type: Observational [Patient Registry]

Aims: to Establish the FLS services at the National Taiwan University Hospital (NTUH) and its Beihu Branch (BB). Method: From Jan., 2014, two related fracture liaison services (FLSs) following the 13 'Capture the Fracture Best Practice Standards' were implemented at the National Taiwan University Hospital (NTUH) health care system. The main hospital (MH) program enrolled patient with 1) new hip fracture 2) newly identified radiographic vertebral fractures or 3) clinical vertebral fractures from both inpatients and outpatients. The Beihu branch (BB) program enrolled only the later two types of patients from outpatients. During the whole study period, two programs planed to enroll 600 fracture patients. Each patient would be assessed at baseline, and every 4 month for at least one year.

NCT ID: NCT02194101 Not yet recruiting - Femoral Fractures Clinical Trials

Supernormal Goal for Proximal Femur Fracture

Start date: August 2014
Phase: N/A
Study type: Observational

This is an observational pilot study of supernormal oxygen delivery goal for patients with proximal femoral fracture.

NCT ID: NCT02190903 Completed - Delirium Clinical Trials

A Trial To Assess Risk of Delirium in Older Adults Undergoing Hip Fracture Surgery With Spinal or General Anesthesia

Start date: October 2013
Phase: N/A
Study type: Interventional

This pilot project will address the gaps in knowledge regarding the effect of anesthetic technique on the risk of delirium through an adequately-powered trial employing standardized regimens for treatment and outcome assessment to test the hypothesis that use of spinal versus general anesthesia decreases the risk of delirium after hip fracture surgery.

NCT ID: NCT02190435 Completed - Clinical trials for Intertrochanteric Femur Fractures

Computer-Assisted Navigation for Intramedullary Nail Fixation of Intertrochanteric Femur Fractures

Start date: July 2014
Phase: N/A
Study type: Interventional

There are approximately 250,000 hip fractures in the US every year, and intertrochanteric (IT) fractures (fractures that occur just below the femoral head) account for nearly half of these fractures. The use of intramedullary (IM) nails for fixation of IT femur fractures has become a well-accepted and increasingly more common procedure among orthopaedic traumatologists, and is standard of care at our institution. While advancements in intramedullary nail fixation have made it a relatively efficient procedure, the placement of the lag screw into the femoral head still remains a challenging step in the procedure. Inaccurate placement can lead to screw cut-out, one of the most commonly reported complications with IM nail fixation. Previous work has shown that the lag screw position is an important factor in reducing screw cut-out. This step of the procedure can be time demanding and often requires several intraoperative radiographs for accurate placement. Recently developed computer-assisted navigation systems provide surgeons with the ability to track screw placement in real-time. This could allow for improved screw placement and potentially reduce radiation exposure to the patient and surgeon. To date, the potential advantages of computer-assisted navigation have not been examined. The primary objective of this study is to examine whether the use of Stryker's ADAPT computer-assisted navigation for Gamma nail fixation can result in improved lag screw placement. The secondary objective is to examine whether the use of the ADAPT for Gamma nail fixation can reduce intraoperative radiation exposure.Our hypothesis is that there is a difference in the lag screw placement (i.e. tip to apex distance measurement) between procedures using the ADAPT system versus the conventional technique for Gamma nail fixation. Additionally, we hypothesize that there is a difference in radiation exposure (i.e. fluoroscopy time) between procedures using the ADAPT system versus the conventional technique for Gamma nail fixation.

NCT ID: NCT02188836 Completed - Clinical trials for Fracture, Closed, Comminuted, Healing

Electromagnetic Stimulation as Coadjuvant in the Healing of Diaphyseal Femoral Fractures

Start date: January 2008
Phase: Phase 3
Study type: Interventional

This study specifically evaluates the effects of electromagnetic stimulation for diaphyseal femur fractures using a device developed by the investigators. The hypothesis is that patients with femoral diaphysis treated with the electromagnetic stimulation have less non-union after six months than patients treated with a placebo device.

NCT ID: NCT02179697 Withdrawn - Spinal Fractures Clinical Trials

Randomized Trial With an Observational Component of Non-operative Versus Operative Treatment for AO Type A3 Fractures

Start date: August 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to compare surgery plus bracing versus bracing alone. Both groups are considered standard of care treatments. The goal of this study is to determine which group is a better treatment.