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Fractures, Bone clinical trials

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NCT ID: NCT03130673 Completed - Hip Fractures Clinical Trials

Challenges of Hip Fracture Care in Developing Countries. Experience at a Level 3 Center in Panama

Start date: September 1, 2014
Phase:
Study type: Observational

An observational study using the information records at the Hospital Regional Rafael Hernandez, in Chiriqui, Panama, that will help to analyze the epidemiology and early treatments results of hip fracture patients treated in this institution.

NCT ID: NCT03126474 Completed - Clinical trials for Distal Radius Fracture

Defining Displacement Thresholds for Surgical Intervention for Distal Radius Fractures - a Delphi Study

Start date: February 17, 2017
Phase:
Study type: Observational

Wrist (distal radius fractures) are very common injuries. Despite this there is still much controversy about the best way to treat them and in particular which ones require intervention. Many studies have been carried out but there is no strong evidence to answer these questions. The investigators are carrying out a Delphi study which involves seeking consensus from experts at treating these injuries about the best way to manage them. UK and international expert surgeons will take part in three rounds of online questionnaires to help decide how much displacement of the fracture will trigger treatment for different common wrist fracture cases. The aim of the study is to obtain expert opinion through consensus from the expert group about the amount of displacement that is acceptable until intervention is required. This will provide guidance and reduce variation between treating surgeons.

NCT ID: NCT03126175 Completed - Clinical trials for Distal Radius Fracture

Above-versus Below-elbow Casting for Conservative Treatment of Distal Radius Fractures

Start date: April 2, 2018
Phase: N/A
Study type: Interventional

For the non-surgical treatment of distal radius fractures in adults a variety cast options are available, including or not the elbow joint. The literature is inconclusive regarding the need to immobilize the elbow joint after reduction of the distal radius fracture.This study was undertaken to evaluate the best method of immobilization between the above and below-elbow cast groups at the end of 6 months of follow-up.

NCT ID: NCT03117868 Completed - Morality Clinical Trials

Mortality of Patients Undergoing Fracture of the Upper Extremity u Femur at the University Hospital of Amiens

FESF-Amiens
Start date: June 2, 2016
Phase:
Study type: Observational

Fractures of the upper femur (EFSF) represent a major public health problem in the elderly. Approximately 1.6 million patients are victims each year of an EFSF and this number is increasing as a result of the aging of the population. In a recent Amiens retrospective study the mortality was estimated to be 22.5% at 1 year of the fracture. In surviving patients, the impact on loss of autonomy and degradation of quality of life is considerable. The reduction of the incidence of post-operative complications includes the identification of risk factors. No prospective study in Amiens has investigated the mortality and the study of the variables involved in the prognosis and long-term mortality of these patients.

NCT ID: NCT03112447 Completed - Fracture Arm Clinical Trials

Treatment of Medial Humeral Epicondyle Fractures in Children With Absorbable Cartilage Nails

Start date: August 1, 2007
Phase: N/A
Study type: Interventional

To compare surgical outcomes from medial epicondyle fracture fixation with absorbable cartilage nails to those from traditional Kirschner wire fixation.

NCT ID: NCT03108716 Completed - Fractures, Bone Clinical Trials

Hamate Hook Removal, Microscrew Internal Fixation and Plaster Fixation for the Treatment of Hamate Hook Fractures

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

To compare the effects of hamate hook removal, microscrew internal fixation and plaster fixation on fracture healing, work, life, and exercise recovery in patients with hamate hook fractures by retrospective case analysis.

NCT ID: NCT03087396 Completed - Stress Fracture Clinical Trials

A Longitudinal Outcomes Study of the Subchondroplasty® Procedure in the Foot/Ankle

Start date: March 10, 2017
Phase:
Study type: Observational

Post Market clinical outcomes study to collect data on the short - and long-term outcomes for subjects who are undergoing or who have undergone the Subchondroplasty Procedure in the foot and/or ankle in a standard clinical setting. Outcomes to be assessed include pain medication usage, pain, function, activity levels and patient satisfaction.

NCT ID: NCT03082872 Completed - Finger Fracture Clinical Trials

Cemented K-wire Fixation vs Open Transfixion Pinning

Start date: January 1, 2009
Phase: N/A
Study type: Interventional

To introduce a novel external-fixation technique using the combination of K-wires and cement, and the objective of this report is also to compare the technique with conventional open transfixion pinning.

NCT ID: NCT03082417 Completed - Pain, Acute Clinical Trials

The PAINFREE Initiative, a Stepped Wedge Cluster Randomized Trial

PAINFREE
Start date: March 1, 2016
Phase: N/A
Study type: Interventional

The PAINFREE (Improving PAIN control following FRactures; towards an Elder-friendly Emergency department) Initiative is a patient-centered multifaceted intervention which aims to improve pain management in patients 75 years and older presenting with a fracture at 7 Emergency Department of participating Montreal hospitals: 1. Montreal General Hospital 2. Royal Victoria Hospital 3. Ste Mary's Hospital 4. Hôpital de Verdun 5. Hôpital du Sacré-Coeur de Montréal 6. Jewish General Hospital 7. Lakeshore General Hospital

NCT ID: NCT03076138 Completed - Bone Loss Clinical Trials

Gene-activated Bone Substitute for Maxillofacial Bone Regeneration

Start date: March 6, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of the gene-activated bone substitute consisting of octacalcium phosphate and plasmid DNA encoding vascular endothelial growth factor (VEGF) for maxillofacial bone regeneration. The patients with congenital and acquired maxillofacial bone defects and alveolar ridge atrophy will be enrolled.