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Fractures, Bone clinical trials

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NCT ID: NCT02614690 Completed - Clinical trials for Fracture of Upper Limb, Level Unspecified

Is Univalving or Bivalving of Long Arm Casts for Forearm Fractures Necessary?

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

This study aims to examine the need for univalve or bivalve splitting of casts in pediatric patients with forearm fractures following closed reduction and cast application in a randomized, prospective fashion.

NCT ID: NCT02609347 Completed - Ankle Fracture Clinical Trials

Manual Therapy After Ankle/Hindfoot Fractures

Start date: November 2015
Phase: N/A
Study type: Interventional

The aim of this randomized controlled trial is to assess if manual therapy improves mobility, gait, and balance more than a control group for patients who have undergone open reduction internal fixation (ORIF) after an ankle/hindfoot fracture.

NCT ID: NCT02609074 Completed - Bone Fracture Clinical Trials

Pilot Clinical Trial of CPC/rhBMP-2 Microffolds as Bone Substitute for Bone Regeneration

Start date: March 2013
Phase: Phase 4
Study type: Interventional

Objective: The investigators initiated a pilot clinical study to test safety and preliminary efficacy in humans (bone tissue repairing capacity) and to evaluate standard clinical and rehabilitation protocols. Summary Background Data: Bone tissue engineering scaffolds loading growth factors have been considered as the most perspective among all bone substitutes, yet little progress of its clinical translation has been made. The concept of "micro-scaffolds" was proposed in this study to provide a trajectory to its clinical translation. Methods: Pre-cured CPC/rhBMP-2 micro-scaffolds have been successfully developed and further applied as an easy-to-operate filler for bone regeneration in a pilot clinical study. Patients of tibial plateau fractures, proximal humeral fractures, or calcaneal fractures at a similar level of severity were randomly divided into two groups and treated by CPC/rhBMP-2 microffolds or traditional CPC paste (control group).

NCT ID: NCT02608801 Completed - Hip Fractures Clinical Trials

Prediction and Secondary Prevention of Fractures

NOFRACTsub
Start date: April 2015
Phase:
Study type: Observational

The purpose of this study is to investigate patient related factors that contribute to increased risk of recurrent fractures and to investigate patient adherence to prescribed anti-osteoporotic drugs.

NCT ID: NCT02608541 Completed - Rib Fractures Clinical Trials

Sheffield Multiple Rib Fractures Study:

SMuRFS
Start date: October 12, 2015
Phase:
Study type: Observational

An observational study to derive clinically relevant and predictive rib fracture classification systems, based on retrospective and prospective cohorts, incorporating assessment of PROMs (Patient Reported Outcome Measures) and healthcare utilisation

NCT ID: NCT02599441 Completed - Clinical trials for Supination-external Rotation Ankle Fractures

Computed Tomography for Evaluating Supination-external Rotation Type Ankle Fractures

Start date: February 2016
Phase:
Study type: Observational

To compare measures of ankle stability from an investigational cone beam computed tomography scanner to gravity stress X-ray in patients who have unstable supination-external rotation ankle fractures.

NCT ID: NCT02591342 Completed - Hip Fracture Clinical Trials

Comparison of a Cemented, Polished Tapered Stem and an Anatomic Stem for Femoral Neck Fracture

Start date: September 2009
Phase: N/A
Study type: Observational

Postoperative periprosthetic femoral fracture after hip arthroplasty is associated with considerable morbidity and mortality. Recent cohort studies have demonstrated a high incidence of PPF in elderly patients treated with two commonly used polished, tapered, collarless stems in elderly patients. The aim of this study was to compare the rate and characteristics of PPF in a consecutive cohort of patients treated either the polished tapered CTP stem or the matte anatomic SP2 stem in an elderly population above 80 years of age with femoral neck fracture.

NCT ID: NCT02591043 Completed - Fracture Clinical Trials

Surgical Treatment of Low Energy Pelvic Fractures in the Elderly

PelvicRetro
Start date: October 2015
Phase: N/A
Study type: Interventional

Since May 2010 the Department of Trauma, Basel University Hospital has performed surgical stabilisation of the posterior pelvic ring on 55 patients. These patients have not received a structured follow up examination or evaluation of outcome after surgery.

NCT ID: NCT02590731 Completed - Hip Fracture Clinical Trials

The Influence of Cognitive Status on Walking Abilities After Femoral Neck Fracture

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

Introduction: Femoral neck fracture is a devastating injury with serious medical and social consequences. One third of these patients have some degree of impaired cognitive status. Despite of this, a high proportion of hip fracture trials exclude patients with cognitive impairment. The investigators aimed to evaluate whether moderate to severe cognitive impairment could predict walking ability, quality of life, functional outcome, reoperations and mortality in elderly patients treated with hemiarthroplasty. Methods: This cohort study included a consecutive series of 188 patients treated with hemiarthroplasty for an displaced femoral neck fracture. Patient were assessed for estimated preoperative and 1 year postoperatively with regard to walking abilities, cognitive status, quality of life with EQ-5D and hip function with Harris hip score.

NCT ID: NCT02589600 Completed - Clinical trials for Osteoporosis, Postmenopausal

Zoledronic Acid for Osteoporotic Fracture Prevention (ZEST II)

ZEST II
Start date: January 2016
Phase: Phase 4
Study type: Interventional

The goal of this study is to perform the first fracture reduction clinical trial with a potent antiresorptive agent (intravenous zoledronic acid) in the most vulnerable long-term care population.