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Femoral Fractures clinical trials

View clinical trials related to Femoral Fractures.

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NCT ID: NCT03185663 Completed - Femoral Fractures Clinical Trials

Pilot Study Comparing Two Techniques of Taking Care Analgesic in Patients 70 and Older, Awaiting Surgery After Extracapsular Fracture of the Proximal Femur

ALGOFRACT
Start date: August 31, 2017
Phase: N/A
Study type: Interventional

The fracture of the proximal femur is a common traumatic pathology in patients aged over 70 years, associated with a mortality of 20 to 30% a year. The care is delayed emergency. During this wait, the occurrence of heel pressure ulcers is regularly found, despite wearing antiescarres slippers. Mobilization, source of pain, is also problematic. 759/5000

NCT ID: NCT03167099 Completed - Clinical trials for Closed Supracondylar Fracture of Femur

Immediate Weight Bearing Versus Protected Weight Bearing in Supracondylar Distal Femur Fractures

WtBrFemFx
Start date: April 2015
Phase: N/A
Study type: Interventional

This study is designed to examine if immediate weight bearing on a distal femur fracture fixed with a primary locking plate, either a distal condylar locking plate or a LISS (less invasive stabilization system), is safe and promotes more rapid fracture healing than partial weight bearing, which is standard of care.

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: NCT02983344 Completed - Femoral Fracture Clinical Trials

Analgesia For Positioning Patient With Femur Fracture For Spinal Anaesthesia

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

This study is performed to determine the efficacy of ultrasound-guided fascia iliaca compartment block during positioning for spinal anaesthesia in patient undergoing repair of proximal femur fracture surgery comparing with intravenous fentanyl.

NCT ID: NCT02848599 Completed - Clinical trials for Postoperative Cognitive Dysfunction

The Influence of Postoperative Analgesia on Systemic Inflammatory Response and POCD After Femoral Fractures Surgery

Start date: July 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether epidural levobupivacaine applied for the purpose of post-operative analgesia compared to systemic analgesia with morphine leads to better pain control, stronger suppression of the inflammatory response and the production of inflammatory mediators, faster recovery of patients and consequently less incidence of postoperative cognitive dysfunction (POCD) in elderly patients after surgical treatment of femoral fractures.

NCT ID: NCT02793947 Completed - Pain, Postoperative Clinical Trials

Efficacy of Peri-Incisional Multimodal Drug Injection Following Operative Management of Femur Fractures

Start date: May 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the efficacy and safety of a peri-incisional multimodal injection for post-operative pain control following operative management of femur fractures. Enrolled subjects will be prospectively randomized into either the peri-incisional injection or control cohorts. Patients will be treated with standard of care surgical techniques by the treating orthopaedic surgeon for the patient's specific fracture pattern. The patients randomized into the injection cohort will receive an intra-operative injection with 400 mg ropivacaine, 0.6 mg epinephrine, 5 mg and morphine into the local superficial and deep peri-incisional tissues while under general anesthesia. Visual analog pain scores will be collected every 4 hours after surgery for the first two post-operative days. Total narcotic consumption will also be recorded over eight hour intervals for the first two post-operative days. Medication related side effects will be monitored. The investigators hypothesize that the peri-incisional injection cohort will demonstrate an improved pain profile and utilize less parenteral narcotic analgesia in the early post-operative period.

NCT ID: NCT02731040 Completed - Osteoporosis Clinical Trials

Exome Sequencing for Atypical Femoral Fractures

Start date: April 2016
Phase:
Study type: Observational

The purpose of this study is to determine whether women who have atypical subtrochanteric and diaphyseal femoral fractures after treatment with bisphosphonates for osteoporosis, have a genetic predisposition to these unusual fractures.

NCT ID: NCT02696915 Completed - Clinical trials for Proximal Femur Fractures

Fascia Iliaca Compartment Block for Proximal-end Femur Fractures

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

Fracture femur is a common injury which is associated with excruciating pain. Positioning for neuraxial blocks is always challenging because even slight overriding of the fracture ends is intensely painful .It can causing major patient distress which accompanied by well-known physiological sequelae such as sympathetic activation causing tachycardia, hypotension, and increased cardiac work that may compromise high-risk cardiac patients. Fascia iliaca compartment block is highly effective in blocking lateral cutaneous nerve of the thigh and femoral nerve. Fascia iliaca compartment block is not only easy to perform but it is also associated with minimal risk as the local anesthetic is injected at a safe distance from the femoral artery and femoral nerve. It is always safe to perform the fascia iliaca compartment block prior to spinal anesthesia as the patient can respond during administration of the local anesthetic and can prevent intra-neuronal injections

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: NCT02475941 Completed - Clinical trials for Distal Femur Fractures

Early Weight Bearing on Supracondylar Distal Femur Fractures in Elderly Patients

Start date: May 11, 2016
Phase: N/A
Study type: Interventional

The investigators will be looking at geriatric distal femur fractures. The investigators will prospectively enroll these patients and allow patients to either weight bear as tolerated or limit their weight bearing post operatively. The investigators will evaluate functional outcomes.