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Femoral Neck Fractures clinical trials

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NCT ID: NCT02057601 Completed - Postoperative Pain Clinical Trials

Postoperative Analgesia for Fractured Neck of Femur With Periarticular Infiltration of Local Anaesthetic

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

The purpose of this study is to determine that periarticular levobupivacaine infiltration after surgical fixation of fractured neck of femur will improve the early postoperative pain sensation.

NCT ID: NCT02030431 Terminated - Clinical trials for Femoral Neck Fracture

Dynaloc for Treatment of Femoral Neck Fractures

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

A prospective, randomized study comparing the effectiveness of a new system, Dynaloc compared with three cancellous screws, for osteosynthesis of femoral neck fractures

NCT ID: NCT02028468 Completed - Clinical trials for Femoral Neck Fracture

Anterolateral Watson Jones Approach Versus Transgluteal Approach for Uncemented Hemi- Arthroplasty in Displaced Femoral Neck Fracture

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

Hemiarthroplasty is a well established treatment of Femoral Neck Fractures in the Elderly. During the last decade the use of Minimal Invasive Surgical( MIS) approaches have been increasing. Our hypothesis is that Patients with a Femoral Neck Fracture may benefit from a MIS approach.

NCT ID: NCT01934049 Recruiting - Clinical trials for Postoperative Complications

Postoperative Recovery in Elderly Patients Undergoing Hip Hemi-arthroplasty

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

Hip fractures incidence grows rapidly with the aging of the population. After indicated surgical treatment, hip fracture patients experience high rates of postoperative complications, postoperative delirium (PD), postoperative cognitive dysfunction (POCD), leading to poor postoperative recovery during hospitalization, which can cause disability, distress for both patients and their families, are associated with other medical complications and account for significant additional health care costs. We currently use dexmedetomidine in elderly patients with hip fractures undergoing hip hemi-arthroplasty in order to improve postoperative recovery and prevent and treating PD and POCD. Dexmedetomidine is a drug used for sedation in critically ill patients that provides some pain relief and controls the bodies response to stress. The sedation produced by dexmedetomidine appears more similar to natural sleep than any other drug used for anesthesia and postoperative sedation. Data suggesting that dexmedetomidine can prevent delirium following cardiac surgery and the developing understanding of the causes of PD and POCD suggest that dexmedetomidine will be particularly effective.

NCT ID: NCT01922622 Completed - Clinical trials for Minimum Effective Dose of Local Anaesthetic With Fentanyl

Minimum Effective Intrathecal Dose of Local Anaesthetic With Fentanyl for Fractured Neck of Femur(Dose Finding Study).

Start date: July 2013
Phase: N/A
Study type: Observational

Fractured neck of femur (FNF) is a common cause of admission to hospital in elderly patients with multiple comorbidities. Anaesthetic management of this patient group is extremely challenging.Neuraxial anaesthesia with minimum doses of local anaesthetic agents administered via a spinal catheter leads to better cardiovascular stability.The minimum dose of local anaesthetic with intrathecal fentanyl was not established yet.We propose to study and determine the initial minimum local anaesthetic dose (MLAD) of 0.5% bupivacaine with 20 mcg of fentanyl administered via a spinal catheter to achieve a sensory block up to T10 for the operative fixation of FNF.We will use a previously well established Dixon and Massey "up-and-down method" to calculate initial MLAD in this prospective, observational trial. Objectives: We would like to determine the initial MLAD of 0.5% bupivacaine with 20mcg of fentanyl administered via a spinal catheter required to achieve a sensory block up to T10 on the side of FNF. Outcomes Primary outcome: 1. Initial MLAD of 0.5% bupivacaine with 20mcg of fentanyl required for a sensory block up to T10 on the side of FNF. Secondary outcomes: 2. Total dose of 0.5% bupivacaine with 20mcg of fentanyl required for the operative fixation of fractured neck of femur. 3. The effect on haemodynamic variables (blood pressure, heart rate). 4. Incidence of side effects 5. The length of postoperative analgesia (the time from the last dose of local anaesthetic administered intrathecally to VAS>3). 6. The time to first rescue analgesic requirement Study Design Prospective, observational trial. Study Size Based on the previously well established Dixon and Massey "up-and-down method"(10), we will recruit patients until a successful spinal block has been achieved in six consecutive patients who received a specific dose. This is the requirement to calculate the initial MLAD.

NCT ID: NCT01908751 Terminated - Clinical trials for Femoral Neck Fractures

Fixation Using Alternative Implants for the Treatment of Hip Fractures (FAITH-2)

FAITH-2
Start date: September 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the impact of surgical fixation (cancellous screws versus sliding hip screws) and biologic intervention (Vitamin D versus placebo) on patient important outcomes.

NCT ID: NCT01844544 Completed - Clinical trials for Femoral Neck Fractures

Drug Related Problems Among Patients With Femoral Neck Fractures in an Orthopedic Ward

Start date: June 2013
Phase: N/A
Study type: Observational [Patient Registry]

the purpose of the study is to: 1. Identify and characterize drug related problems in patients after a femur neck fracture that are hospitalized in the orthopedic department at "Meir" medical center. 2. Evaluate the contribution of a clinical pharmacist in identifying,characterizing and preventing drug related problems in patients after a femur neck fracture that are hospitalized in the orthopedic department at "Meir" medical center.

NCT ID: NCT01807039 Completed - Clinical trials for Fracture of Neck of Femur (Hip)

Mortality Following Surgery for Proximal Femoral Fractures

HipMo
Start date: December 2012
Phase: N/A
Study type: Observational

Proximal femoral fractures are most frequent traumatologic and orthopedic diagnoses undergoing surgery. It affect most seniors and accompanied by a series of complications. The aim of our retrospective clinical trial is to establish a thirty-day mortality rate after surgical solutions, mortality during hospitalization and compare the types of anesthesia chosen during the performance (general vs. subarachnoid anesthesia).

NCT ID: NCT01798472 Recruiting - Clinical trials for Femoral Neck Fractures

Hip Fractures Treated With Uncemented Arthroplasties

HUA
Start date: November 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to compare the functional and radiological outcome after displaced, femoral neck fractures treated with either cemented or uncemented arthroplasties. The primary hypothesis is that the uncemented arthroplasty shows the same functional outcome at 12 month as the cemented arthroplasty.

NCT ID: NCT01787929 Completed - Clinical trials for Femoral Neck Fractures

Displaced Femoral Neck Fracture in Elderly Patient. Should Cement be Used for Hip Hemiarthroplasty ?

PIH
Start date: February 7, 2016
Phase: N/A
Study type: Interventional

The purpose of this study was to identify the clinical relevance of cementless hemiarthroplasties, compare Harris functional score.The hypothesis is the non-inferiority of cementless hemiarthroplasties compare cemented hemiarthroplasties in order to justify the relevance of cementless hemiarthroplasties in displaced femoral neck fractures. 150 patients will be included, 75 with cemented hemiarthroplasty and 75 with uncemented hemiarthroplasty. They will be followed during one year after the surgery, with a functionality assessment at 3 month and 12 month.